A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528756



Internal ID15109363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4034049..4069115hg38UCSC Ensembl
Innerchr3:4075733..4110799hg19UCSC Ensembl
Innerchr3:4050733..4085799hg18UCSC Ensembl
Innerchr3:4050733..4085799hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3835067
hg1935067
hg1835067
hg1735067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705418
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528756
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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