A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520181



Internal ID15100788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108912490..108913648hg38UCSC Ensembl
Innerchr3:108631337..108632495hg19UCSC Ensembl
Innerchr3:110114027..110115185hg18UCSC Ensembl
Innerchr3:110114027..110115185hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg381159
hg191159
hg181159
hg171159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675471, nssv690016, nssv661444, nssv679245
Samples
Known GenesGUCA1C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520181
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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