A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756070



Internal ID16050026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100439122..100446332hg38UCSC Ensembl
Innerchr10:102198879..102206089hg19UCSC Ensembl
Innerchr10:102188869..102196079hg18UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg387211
hg197211
hg187211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552050
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv756070
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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