A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747424



Internal ID15694694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46325178hg38UCSC Ensembl
Innerchr10:47543322..47696414hg19UCSC Ensembl
Innerchr10:47013328..47166420hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38153093
hg19153093
hg18153093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550750
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747424
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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