A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696286



Internal ID15432938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25261856..25292597hg38UCSC Ensembl
Innerchr4:25263478..25294219hg19UCSC Ensembl
Innerchr4:24872576..24903317hg18UCSC Ensembl
Innerchr4:24939747..24970488hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3830742
hg1930742
hg1830742
hg1730742
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518834
Supporting Variants
Samples
Known GenesPI4K2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696286
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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