A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3892584

Internal ID

18836718

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr14:105708865..106115912	hg38	UCSC Ensembl
Outer	chr14:105581568..106470101	hg38	UCSC Ensembl
Inner	chr14:106175202..106572510	hg19	UCSC Ensembl
Outer	chr14:106047905..106926025	hg19	UCSC Ensembl
Inner	chr14:105246247..105643555	hg18	UCSC Ensembl
Outer	chr14:105118950..105997070	hg18	UCSC Ensembl

Cytoband

14q32.33

Allele length

Assembly	Allele length
hg38	888534
hg19	878121
hg18	878121

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

essv25790162, essv25791959, essv25791493, essv25792387, essv25792303, essv25790921, essv25791904, essv25791978, essv25791946, essv25791024, essv25790737, essv25789750, essv25791525, essv25790436, essv25791474, essv25791179, essv25792252, essv25790918, essv25791890, essv25790606, essv25790304, essv25792006, essv25791935, essv25789677, essv25791963, essv25792344, essv25791301, essv25791926, essv25791651, essv25792378, essv25791515, essv25791563, essv25791131, essv25791133, essv25791090, essv25791544, essv25790394, essv25790666, essv25791590, essv25791764, essv25791500, essv25791693, essv25790920, essv25791540, essv25790370, essv25790995, essv25790315, essv25791263, essv25791551, essv25791460, essv25791985, essv25790702, essv25791641, essv25791943, essv25790127, essv25791752, essv25791566, essv25791554, essv25790760, essv25791039, essv25791355, essv25791779, essv25790660, essv25791477, essv25791306, essv25791397, essv25791957, essv25791805, essv25791095, essv25792190, essv25792306, essv25792093, essv25790618, essv25791924, essv25791437, essv25791505, essv25791860, essv25790057, essv25791634, essv25791730, essv25791173, essv25791219, essv25792265, essv25791383, essv25791139, essv25791522, essv25790187, essv25791620, essv25790579, essv25791483, essv25791084, essv25791329, essv25791135, essv25791035, essv25792316, essv25791452, essv25791182, essv25791016, essv25791022, essv25790767, essv25791034, essv25792308, essv25791049, essv25792311, essv25791835, essv25791221, essv25790846, essv25791339, essv25790188, essv25791529, essv25791399, essv25792328, essv25789968

Samples

Known Genes

ADAM6, ELK2AP, KIAA0125, LINC00226, MIR8071-1, MIR8071-2

Method

SNP array

Analysis

Platform

Illumina HumanHap 610

Comments

Reference

Suktitipat_et_al_2014

Pubmed ID

Accession Number(s)

Frequency

Sample Size	3017
Observed Gain	113
Observed Loss	0
Observed Complex	0
Frequency	n/a