A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549953



Internal ID16337362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8891474..9095411hg38UCSC Ensembl
Innerchr10:8933437..9137374hg19UCSC Ensembl
Innerchr10:8973443..9177380hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38203938
hg19203938
hg18203938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743997
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549953
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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