A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174503



Internal ID15530308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46216824..46257656hg38UCSC Ensembl
Innerchr10:47588060..47628892hg19UCSC Ensembl
Innerchr10:47058066..47098898hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3840833
hg1940833
hg1840833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550769
Supporting Variants
SamplesHGDP00924
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174503
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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