A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676666



Internal ID15066632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137259590..137262795hg38UCSC Ensembl
Innerchr4:138180744..138183949hg19UCSC Ensembl
Innerchr4:138400194..138403399hg18UCSC Ensembl
Innerchr4:138538349..138541554hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg383206
hg193206
hg183206
hg173206
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516176
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676666
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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