A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749779



Internal ID16043735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65663599..65713987hg38UCSC Ensembl
Innerchr10:67423357..67473745hg19UCSC Ensembl
Innerchr10:67093363..67143751hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3850389
hg1950389
hg1850389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551291
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)nssv749779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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