A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652181



Internal ID15388833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:153020470..153024191hg38UCSC Ensembl
Innerchr4:153941622..153945343hg19UCSC Ensembl
Innerchr4:154161072..154164793hg18UCSC Ensembl
Innerchr4:154299227..154302948hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383722
hg193722
hg183722
hg173722
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517491
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652181
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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