A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175010



Internal ID15531983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110819541..110852713hg38UCSC Ensembl
Innerchr10:112579299..112612471hg19UCSC Ensembl
Innerchr10:112569289..112602461hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3833173
hg1933173
hg1833173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552172
Supporting Variants
SamplesHGDP01238
Known GenesRBM20
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175010
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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