A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698386



Internal ID15088352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143908753..143973107hg38UCSC Ensembl
Innerchr4:144829906..144894260hg19UCSC Ensembl
Innerchr4:145049356..145113710hg18UCSC Ensembl
Innerchr4:145187511..145251865hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3864355
hg1964355
hg1864355
hg1764355
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517006
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698386
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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