A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549991



Internal ID16337400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13528082..13529347hg38UCSC Ensembl
Innerchr10:13570082..13571347hg19UCSC Ensembl
Innerchr10:13610088..13611353hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381266
hg191266
hg181266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744067, nssv744068
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549991
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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