A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523029



Internal ID15103636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45872959..45876389hg38UCSC Ensembl
Innerchr19:46376217..46379647hg19UCSC Ensembl
Innerchr19:51068057..51071487hg18UCSC Ensembl
Innerchr19:51068057..51071487hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383431
hg193431
hg183431
hg173431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698710
Samples
Known GenesFOXA3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523029
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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