A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528019



Internal ID15455312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:174700122..174708919hg38UCSC Ensembl
Innerchr3:174417912..174426709hg19UCSC Ensembl
Innerchr3:175900606..175909403hg18UCSC Ensembl
Innerchr3:175900614..175909411hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg388798
hg198798
hg188798
hg178798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704548
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528019
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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