A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015600



Internal ID19104817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57487712..57636411hg38UCSC Ensembl
Innerchr8:58400271..58548970hg19UCSC Ensembl
Innerchr8:58562825..58711524hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38148700
hg19148700
hg18148700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7232n100
Supporting Variantsnssv3689450
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015600
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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