A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021805



Internal ID18764339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39540952hg38UCSC Ensembl
Innerchr8:39235591..39398471hg19UCSC Ensembl
Innerchr8:39354748..39517628hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38162881
hg19162881
hg18162881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7166n100
Supporting Variantsnssv3687602, nssv3687601
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)nsv1021805
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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