A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668516



Internal ID15405168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65303925..65311056hg38UCSC Ensembl
Innerchr4:66169643..66176774hg19UCSC Ensembl
Innerchr4:65852238..65859369hg18UCSC Ensembl
Innerchr4:65998409..66005540hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg387132
hg197132
hg187132
hg177132
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516455
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668516
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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