A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677968



Internal ID15414620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31692769..31711322hg38UCSC Ensembl
Innerchr5:31692876..31711429hg19UCSC Ensembl
Innerchr5:31728633..31747186hg18UCSC Ensembl
Innerchr5:31728633..31747186hg17UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3818554
hg1918554
hg1818554
hg1718554
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515637
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677968
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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