A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525574



Internal ID15452867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:5540407..5553725hg38UCSC Ensembl
Innerchr2:5680539..5693857hg19UCSC Ensembl
Innerchr2:5597990..5611308hg18UCSC Ensembl
Innerchr2:5631137..5644455hg17UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3813319
hg1913319
hg1813319
hg1713319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701713
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525574
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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