A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527126



Internal ID15454419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:134423251..134425077hg38UCSC Ensembl
Innerchr3:134142093..134143919hg19UCSC Ensembl
Innerchr3:135624783..135626609hg18UCSC Ensembl
Innerchr3:135624791..135626617hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381827
hg191827
hg181827
hg171827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703511
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527126
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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