A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700938



Internal ID15437590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25277366..25294382hg38UCSC Ensembl
Innerchr4:25278988..25296004hg19UCSC Ensembl
Innerchr4:24888086..24905102hg18UCSC Ensembl
Innerchr4:24955257..24972273hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3817017
hg1917017
hg1817017
hg1717017
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524925
Supporting Variants
Samples
Known GenesPI4K2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700938
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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