A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525627



Internal ID15106234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:123175406..123254659hg38UCSC Ensembl
Innerchr3:122894253..122973506hg19UCSC Ensembl
Innerchr3:124376943..124456196hg18UCSC Ensembl
Innerchr3:124376943..124456196hg17UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3879254
hg1979254
hg1879254
hg1779254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv297n21
Supporting Variantsnssv701776
Samples
Known GenesSEC22A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525627
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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