A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551292



Internal ID16338701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65663599..65714157hg38UCSC Ensembl
Innerchr10:67423357..67473915hg19UCSC Ensembl
Innerchr10:67093363..67143921hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3850559
hg1950559
hg1850559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1220n54
Supporting Variantsnssv749780
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551292
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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