A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526275



Internal ID15453568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52028459..52089160hg38UCSC Ensembl
Innerchr2:52255597..52316298hg19UCSC Ensembl
Innerchr2:52109101..52169802hg18UCSC Ensembl
Innerchr2:52167248..52227949hg17UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3860702
hg1960702
hg1860702
hg1760702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702553
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526275
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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