A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685161



Internal ID18983442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39461682hg38UCSC Ensembl
Innerchr8:39235591..39319201hg19UCSC Ensembl
Innerchr8:39354748..39438358hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3883611
hg1983611
hg1883611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024707
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)nssv3685161
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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