A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698777



Internal ID15435429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28955692..29145548hg38UCSC Ensembl
Innerchr5:28955799..29145655hg19UCSC Ensembl
Innerchr5:28991556..29181412hg18UCSC Ensembl
Innerchr5:28991556..29181412hg17UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38189857
hg19189857
hg18189857
hg17189857
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523085
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698777
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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