A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702411



Internal ID15439063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:38735182..38737781hg38UCSC Ensembl
Innerchr5:38735284..38737883hg19UCSC Ensembl
Innerchr5:38771041..38773640hg18UCSC Ensembl
Innerchr5:38771041..38773640hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg382600
hg192600
hg182600
hg172600
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526152
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702411
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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