A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698206



Internal ID15434858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:119672720..119680118hg38UCSC Ensembl
Innerchr5:119008415..119015813hg19UCSC Ensembl
Innerchr5:119036314..119043712hg18UCSC Ensembl
Innerchr5:119036314..119043712hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg387399
hg197399
hg187399
hg177399
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521588
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698206
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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