A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1040575



Internal ID15893761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:117707064..117784749hg38UCSC Ensembl
Innerchr5:117042759..117120444hg19UCSC Ensembl
Innerchr5:117070658..117148343hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3877686
hg1977686
hg1877686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599489
Supporting Variants
Samples
Known GenesLOC102467224
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1040575
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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