A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173574



Internal ID15532975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46269108hg38UCSC Ensembl
Innerchr10:47543322..47640344hg19UCSC Ensembl
Innerchr10:47013328..47110350hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3897023
hg1997023
hg1897023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550741
Supporting Variants
SamplesHGDP01413
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173574
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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