A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749984



Internal ID15697254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67805187..67937238hg38UCSC Ensembl
Innerchr10:69564945..69696995hg19UCSC Ensembl
Innerchr10:69234951..69367001hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38132052
hg19132051
hg18132051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551433
Supporting Variants
Samples
Known GenesDNAJC12, HERC4, SIRT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv749984
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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