A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519055



Internal ID15446348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153301919..153326431hg38UCSC Ensembl
Innerchr3:153019708..153044220hg19UCSC Ensembl
Innerchr3:154502398..154526910hg18UCSC Ensembl
Innerchr3:154502406..154526918hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3824513
hg1924513
hg1824513
hg1724513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696527
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519055
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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