A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526119



Internal ID15453412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:213464140..213478805hg38UCSC Ensembl
Innerchr1:213637483..213652148hg19UCSC Ensembl
Innerchr1:211704106..211718771hg18UCSC Ensembl
Innerchr1:210025878..210040543hg17UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3814666
hg1914666
hg1814666
hg1714666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702369
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526119
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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