A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515699



Internal ID15443310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22590102..22599157hg38UCSC Ensembl
Innerchr3:22631593..22640648hg19UCSC Ensembl
Innerchr3:22606597..22615652hg18UCSC Ensembl
Innerchr3:22606597..22615652hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg389056
hg199056
hg189056
hg179056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669513, nssv664458, nssv684279, nssv682605, nssv670485, nssv666789
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515699
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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