A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550233



Internal ID15990956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26679242..26722394hg38UCSC Ensembl
Innerchr10:26968171..27011323hg19UCSC Ensembl
Innerchr10:27008177..27051329hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3843153
hg1943153
hg1843153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744743
Samples
Known GenesPDSS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550233
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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