A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760555



Internal ID18712150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39372652..39531248hg38UCSC Ensembl
Innerchr8:39230171..39388767hg19UCSC Ensembl
Innerchr8:39349328..39507924hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38158597
hg19158597
hg18158597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018777
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3760555
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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