A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689020



Internal ID18987301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39389144..39541712hg38UCSC Ensembl
Innerchr8:39246663..39399231hg19UCSC Ensembl
Innerchr8:39365820..39518388hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38152569
hg19152569
hg18152569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034516
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)nssv3689020
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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