A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685199



Internal ID18983480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39475602hg38UCSC Ensembl
Innerchr8:39235591..39333121hg19UCSC Ensembl
Innerchr8:39354748..39452278hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3897531
hg1997531
hg1897531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021742
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)nssv3685199
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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