A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685627



Internal ID18637222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39368818..39522136hg38UCSC Ensembl
Innerchr8:39226337..39379655hg19UCSC Ensembl
Innerchr8:39345494..39498812hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38153319
hg19153319
hg18153319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029138
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)nssv3685627
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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