A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702062



Internal ID15092028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189125097..189150831hg38UCSC Ensembl
Innerchr4:190046251..190071985hg19UCSC Ensembl
Innerchr4:190283245..190308979hg18UCSC Ensembl
Innerchr4:190421400..190447134hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3825735
hg1925735
hg1825735
hg1725735
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517295
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702062
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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