A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1040574



Internal ID15893760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:117521671..117569357hg38UCSC Ensembl
Innerchr5:116857366..116905052hg19UCSC Ensembl
Innerchr5:116885265..116932951hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3847687
hg1947687
hg1847687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599488
Supporting Variants
Samples
Known GenesLINC00992
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1040574
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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