A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787142



Internal ID19167668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160819809..160836386hg38UCSC Ensembl
Innerchr6:161240841..161257418hg19UCSC Ensembl
Innerchr6:161160831..161177408hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3816578
hg1916578
hg1816578
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890976
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787142
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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