A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174548



Internal ID15876134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78507242..78552650hg38UCSC Ensembl
Innerchr10:80266999..80312407hg19UCSC Ensembl
Innerchr10:79937005..79982413hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3845409
hg1945409
hg1845409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551563
Supporting Variants
SamplesHGDP00788
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174548
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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