A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688704



Internal ID18640299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:56835555..57145097hg38UCSC Ensembl
Innerchr8:57748114..58057656hg19UCSC Ensembl
Innerchr8:57910668..58220210hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38309543
hg19309543
hg18309543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029443
Supporting Variants
Samples
Known GenesIMPAD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688704
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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