A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551290



Internal ID16338699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65663599..65713414hg38UCSC Ensembl
Innerchr10:67423357..67473172hg19UCSC Ensembl
Innerchr10:67093363..67143178hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3849816
hg1949816
hg1849816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1220n54
Supporting Variantsnssv749778
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551290
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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