A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3683188



Internal ID18981469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39505415hg38UCSC Ensembl
Innerchr8:39235591..39362934hg19UCSC Ensembl
Innerchr8:39354748..39482091hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38127344
hg19127344
hg18127344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031323
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)nssv3683188
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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