A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672599



Internal ID15409251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167894196..168066603hg38UCSC Ensembl
Innerchr4:168815347..168987754hg19UCSC Ensembl
Innerchr4:169051922..169224329hg18UCSC Ensembl
Innerchr4:169190077..169362484hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38172408
hg19172408
hg18172408
hg17172408
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515790
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672599
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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