A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524614



Internal ID15105221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:123175405..123223935hg38UCSC Ensembl
Innerchr3:122894252..122942782hg19UCSC Ensembl
Innerchr3:124376942..124425472hg18UCSC Ensembl
Innerchr3:124376942..124425472hg17UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3848531
hg1948531
hg1848531
hg1748531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700575
Samples
Known GenesSEC22A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524614
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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