A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704682



Internal ID15441334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:140788992..140814253hg38UCSC Ensembl
Innerchr4:141710146..141735407hg19UCSC Ensembl
Innerchr4:141929596..141954857hg18UCSC Ensembl
Innerchr4:142067751..142093012hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3825262
hg1925262
hg1825262
hg1725262
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528137
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704682
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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