A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174096



Internal ID15528844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:790175..842133hg38UCSC Ensembl
Innerchr10:836115..888073hg19UCSC Ensembl
Innerchr10:826115..878073hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3851959
hg1951959
hg1851959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549766
Supporting Variants
SamplesHGDP00696
Known GenesLARP4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174096
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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