A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524864



Internal ID15452157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:182524093..182527433hg38UCSC Ensembl
Innerchr3:182241881..182245221hg19UCSC Ensembl
Innerchr3:183724575..183727915hg18UCSC Ensembl
Innerchr3:183724583..183727923hg17UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg383341
hg193341
hg183341
hg173341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv307n21
Supporting Variantsnssv700869
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524864
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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