A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752187



Internal ID16046143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84686643..84707377hg38UCSC Ensembl
Innerchr10:86446399..86467133hg19UCSC Ensembl
Innerchr10:86436379..86457113hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3820735
hg1920735
hg1820735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551758
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)nssv752187
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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