A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015464



Internal ID18757998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39373128..39539496hg38UCSC Ensembl
Innerchr8:39230647..39397015hg19UCSC Ensembl
Innerchr8:39349804..39516172hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38166369
hg19166369
hg18166369
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7166n100
Supporting Variantsnssv3685037, nssv3685039, nssv3685038, nssv3685040, nssv3685041
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)nsv1015464
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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