A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173590



Internal ID15530297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46281263hg38UCSC Ensembl
Innerchr10:47543322..47652499hg19UCSC Ensembl
Innerchr10:47013328..47122505hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38109178
hg19109178
hg18109178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550743
Supporting Variants
SamplesHGDP00923
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173590
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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