A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687811



Internal ID15424463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43329112..43338381hg38UCSC Ensembl
Innerchr14:43798315..43807584hg19UCSC Ensembl
Innerchr14:42868065..42877334hg18UCSC Ensembl
Innerchr14:42868065..42877334hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg389270
hg199270
hg189270
hg179270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515592
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687811
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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