A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687182



Internal ID15423834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17638738..17680982hg38UCSC Ensembl
Innerchr5:17638847..17681091hg19UCSC Ensembl
Innerchr5:17671545..17713838hg18UCSC Ensembl
Innerchr5:17671545..17713838hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3842245
hg1942245
hg1842294
hg1742294
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516462
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687182
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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