A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525219



Internal ID15452512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191471343..191505875hg38UCSC Ensembl
Innerchr3:191189132..191223664hg19UCSC Ensembl
Innerchr3:192671826..192706358hg18UCSC Ensembl
Innerchr3:192671834..192706366hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3834533
hg1934533
hg1834533
hg1734533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701305
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525219
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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