A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053962



Internal ID19143181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42118976..42324825hg38UCSC Ensembl
Innerchr10:42614424..42820273hg19UCSC Ensembl
Innerchr10:41934430..42140279hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38205850
hg19205850
hg18205850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv717n100
Supporting Variantsnssv3707769
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)nsv1053962
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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