A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173572



Internal ID15530318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46252602hg38UCSC Ensembl
Innerchr10:47543322..47623838hg19UCSC Ensembl
Innerchr10:47013328..47093844hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3880517
hg1980517
hg1880517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550738
Supporting Variants
SamplesHGDP00925
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173572
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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