A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785674



Internal ID18828358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31817676..31827305hg38UCSC Ensembl
Innerchr6:31785453..31795082hg19UCSC Ensembl
Innerchr6:31893432..31903061hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg389630
hg199630
hg189630
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890822
Supporting Variants
Samples
Known GenesHSPA1A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785674
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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