Variant Details

Variant: esv3355385

Internal ID

14855649

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr3:2920310..2920322	hg38	UCSC Ensembl
Inner	chr3:2920301..2920331	hg38	UCSC Ensembl
Outer	chr3:2920289..2920340	hg38	UCSC Ensembl
	chr3:2961994..2962006	hg19	UCSC Ensembl
Inner	chr3:2961985..2962015	hg19	UCSC Ensembl
Outer	chr3:2961973..2962024	hg19	UCSC Ensembl
	chr3:2936994..2937006	hg18	UCSC Ensembl
Inner	chr3:2937015..2936985	hg18	UCSC Ensembl
Outer	chr3:2936973..2937024	hg18	UCSC Ensembl

Cytoband

3p26.2

Allele length

Assembly	Allele length
hg38	284
hg19	284
hg18	284

Variant Type

CNV insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv8911567, essv8911544, essv8911575, essv8911621, essv8911580, essv8911578, essv8911560, essv8911618, essv8911532, essv8911596, essv8911620, essv8911624, essv8911638, essv8911540, essv8911608, essv8911626, essv8911617, essv8911564, essv8911551, essv8911583, essv8911571, essv8911545, essv8911562, essv8911552, essv8911542, essv8911539, essv8911619, essv8911543, essv8911639, essv8911556, essv8911593, essv8911554, essv8911561, essv8911538, essv8911632, essv8911611, essv8911635, essv8911533, essv8911555, essv8911615, essv8911605, essv8911577, essv8911606, essv8911601, essv8911588, essv8911569, essv8911553, essv8911584, essv8911541, essv8911537, essv8911587, essv8911612, essv8911610, essv8911548, essv8911640, essv8911550, essv8911572, essv8911549, essv8911585, essv8911628, essv8911586, essv8911573, essv8911576, essv8911594, essv8911600, essv8911599, essv8911613, essv8911589, essv8911604, essv8911557, essv8911622, essv8911563, essv8911590, essv8911598, essv8911629, essv8911582, essv8911623, essv8911616, essv8911630, essv8911565, essv8911546, essv8911597, essv8911633, essv8911637, essv8911631, essv8911627, essv8911591, essv8911634, essv8911535, essv8911566, essv8911609, essv8911574, essv8911602, essv8911534, essv8911607, essv8911568, essv8911595, essv8911579

Samples

NA19137, NA18870, NA18964, NA12154, NA12043, NA12249, NA18861, NA18605, NA12750, NA07037, NA18951, NA18871, NA18561, NA18523, NA18952, NA19114, NA11920, NA18501, NA19093, NA18526, NA11918, NA18550, NA18570, NA18511, NA18545, NA18603, NA18948, NA18516, NA18517, NA18947, NA18573, NA18608, NA18542, NA19210, NA12776, NA07051, NA19257, NA19108, NA18965, NA18505, NA12414, NA18912, NA18508, NA12004, NA18566, NA12155, NA18576, NA18960, NA18563, NA07357, NA18592, NA12761, NA18638, NA18956, NA18959, NA18547, NA11831, NA11894, NA11995, NA18593, NA12751, NA19190, NA12716, NA18537, NA19129, NA18572, NA18498, NA19102, NA06986, NA18522, NA19005, NA18510, NA18502, NA18504, NA18564, NA18858, NA18942, NA18961, NA18562, NA18945, NA18582, NA18552, NA19138, NA18907, NA18909, NA12156, NA19116, NA18577, NA19099, NA11992, NA12003, NA18944, NA19225, NA18499, NA18571, NA11829, NA12717, NA18555

Known Genes

CNTN4

Method

Sequencing

Analysis

Platform

Illumina

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3355385

Frequency

Sample Size	185
Observed Gain	98
Observed Loss	0
Observed Complex	0
Frequency	n/a