A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041712



Internal ID19130931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20501155..20535294hg38UCSC Ensembl
Innerchr10:20790084..20824223hg19UCSC Ensembl
Innerchr10:20830090..20864229hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3834140
hg1934140
hg1834140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv687n100
Supporting Variantsnssv3513351
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)nsv1041712
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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