A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698248



Internal ID15434900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177937883..177969199hg38UCSC Ensembl
Innerchr5:177364884..177396200hg19UCSC Ensembl
Innerchr5:177297490..177328806hg18UCSC Ensembl
Innerchr5:177297490..177328806hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3831317
hg1931317
hg1831317
hg1731317
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521629
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698248
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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