A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526603



Internal ID15453896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4243071..4253667hg38UCSC Ensembl
Innerchr2:4290661..4301257hg19UCSC Ensembl
Innerchr2:4268536..4279132hg18UCSC Ensembl
Innerchr2:3784030..3794626hg17UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3810597
hg1910597
hg1810597
hg1710597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n21
Supporting Variantsnssv702923
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526603
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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