Variant Details

Variant: esv3404133

Internal ID

15251095

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr3:191281661..191281673	hg38	UCSC Ensembl
Inner	chr3:191281652..191281682	hg38	UCSC Ensembl
Outer	chr3:191281640..191281694	hg38	UCSC Ensembl
	chr3:190999450..190999462	hg19	UCSC Ensembl
Inner	chr3:190999441..190999471	hg19	UCSC Ensembl
Outer	chr3:190999429..190999483	hg19	UCSC Ensembl
	chr3:192482144..192482156	hg18	UCSC Ensembl
Inner	chr3:192482165..192482135	hg18	UCSC Ensembl
Outer	chr3:192482123..192482177	hg18	UCSC Ensembl

Cytoband

3q28

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

essv8917087, essv8917122, essv8917108, essv8917082, essv8917104, essv8917097, essv8917126, essv8917071, essv8917053, essv8917076, essv8917078, essv8917049, essv8917054, essv8917079, essv8917055, essv8917075, essv8917064, essv8917115, essv8917077, essv8917107, essv8917123, essv8917090, essv8917060, essv8917085, essv8917059, essv8917051, essv8917070, essv8917096, essv8917067, essv8917119, essv8917093, essv8917046, essv8917127, essv8917118, essv8917083, essv8917044, essv8917056, essv8917048, essv8917045, essv8917061, essv8917099, essv8917081, essv8917098, essv8917063, essv8917086, essv8917109, essv8917100, essv8917117, essv8917052, essv8917110, essv8917105, essv8917084, essv8917120, essv8917057, essv8917066, essv8917043, essv8917089, essv8917112, essv8917073, essv8917111, essv8917106, essv8917094, essv8917068, essv8917050, essv8917074, essv8917042, essv8917088, essv8917072, essv8917116, essv8917095, essv8917121, essv8917062, essv8917101, essv8917103, essv8917124, essv8917065, essv8917092

Samples

NA12717, NA11995, NA11829, NA18861, NA18508, NA10851, NA11920, NA11931, NA12751, NA18959, NA18870, NA12750, NA12155, NA07346, NA18563, NA19005, NA18944, NA18940, NA18960, NA11992, NA11918, NA18571, NA12287, NA18949, NA12761, NA12156, NA12044, NA11994, NA18520, NA18973, NA11993, NA11831, NA10847, NA18951, NA18605, NA12489, NA12003, NA18579, NA18572, NA18907, NA18537, NA18573, NA11919, NA11894, NA12249, NA18912, NA18853, NA19099, NA19257, NA18555, NA12144, NA18523, NA18570, NA18593, NA18576, NA12043, NA18608, NA12716, NA11881, NA19108, NA18961, NA18952, NA18564, NA07037, NA12763, NA06986, NA12749, NA18609, NA18552, NA18505, NA19129, NA12006, NA12154, NA18562, NA12776, NA18965, NA18577

Known Genes

UTS2B

Method

Sequencing

Analysis

Platform

Illumina

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3404133

Frequency

Sample Size	185
Observed Gain	77
Observed Loss	0
Observed Complex	0
Frequency	n/a