A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520614



Internal ID15447907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:14351234..14352231hg38UCSC Ensembl
Innerchr1:14677729..14678726hg19UCSC Ensembl
Innerchr1:14550316..14551313hg18UCSC Ensembl
Innerchr1:14423035..14424032hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38998
hg19998
hg18998
hg17998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697519
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520614
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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