A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760222



Internal ID19058503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16017012..16146893hg38UCSC Ensembl
Innerchr8:15874521..16004402hg19UCSC Ensembl
Innerchr8:15918892..16048773hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38129882
hg19129882
hg18129882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024623
Supporting Variants
Samples
Known GenesMSR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3760222
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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