A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038334



Internal ID19127553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20501155..20542420hg38UCSC Ensembl
Innerchr10:20790084..20831349hg19UCSC Ensembl
Innerchr10:20830090..20871355hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3841266
hg1941266
hg1841266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv687n100
Supporting Variantsnssv3506665, nssv3521938
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)nsv1038334
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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