A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752185



Internal ID16046141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84570457..84592655hg38UCSC Ensembl
Innerchr10:86330213..86352411hg19UCSC Ensembl
Innerchr10:86320193..86342391hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3822199
hg1922199
hg1822199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551755
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)nssv752185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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