A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665878



Internal ID15402530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152135395..152163567hg38UCSC Ensembl
Innerchr5:151514956..151543128hg19UCSC Ensembl
Innerchr5:151495149..151523321hg18UCSC Ensembl
Innerchr5:151495149..151523321hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3828173
hg1928173
hg1828173
hg1728173
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516251
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665878
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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