A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1022097



Internal ID16316053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1178554..1180196hg38UCSC Ensembl
Innerchr5:1178669..1180311hg19UCSC Ensembl
Innerchr5:1231669..1233311hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381643
hg191643
hg181643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596843
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1022097
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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