A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039650



Internal ID19128869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623495..5678549hg38UCSC Ensembl
Innerchr10:5665458..5720512hg19UCSC Ensembl
Innerchr10:5705464..5760518hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3855055
hg1955055
hg1855055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv665n100
Supporting Variantsnssv3498882
Samples
Known GenesASB13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039650
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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