A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518697



Internal ID15445990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:14351234..14362212hg38UCSC Ensembl
Innerchr1:14677729..14688707hg19UCSC Ensembl
Innerchr1:14550316..14561294hg18UCSC Ensembl
Innerchr1:14423035..14434013hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3810979
hg1910979
hg1810979
hg1710979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696148
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518697
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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