A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697443



Internal ID15434095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141519118..141522955hg38UCSC Ensembl
Innerchr4:142440271..142444108hg19UCSC Ensembl
Innerchr4:142659721..142663558hg18UCSC Ensembl
Innerchr4:142797876..142801713hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg383838
hg193838
hg183838
hg173838
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520477
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697443
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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