A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022332



Internal ID19111550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39429596..39537578hg38UCSC Ensembl
Innerchr8:39287115..39395097hg19UCSC Ensembl
Innerchr8:39406272..39514254hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38107983
hg19107983
hg18107983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7180n100
Supporting Variantsnssv3685976
Samples
Known GenesADAM3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022332
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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