A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694808



Internal ID15431460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:13633859..13645879hg38UCSC Ensembl
Innerchr5:13633968..13645988hg19UCSC Ensembl
Innerchr5:13686968..13698988hg18UCSC Ensembl
Innerchr5:13686968..13698988hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3812021
hg1912021
hg1812021
hg1712021
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522038
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694808
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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