A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550546



Internal ID16337955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38782022..38861089hg38UCSC Ensembl
Innerchr10:39075153..39154220hg19UCSC Ensembl
Innerchr10:39115159..39194226hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3879068
hg1979068
hg1879068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1065n54
Supporting Variantsnssv747043
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550546
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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