A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757331



Internal ID19055612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102664742..102716969hg38UCSC Ensembl
Innerchr8:103676970..103729197hg19UCSC Ensembl
Innerchr8:103746146..103798373hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3852228
hg1952228
hg1852228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018625
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3757331
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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