A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668665



Internal ID15405317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101378772..101393317hg38UCSC Ensembl
Innerchr14:101845109..101859654hg19UCSC Ensembl
Innerchr14:100914862..100929407hg18UCSC Ensembl
Innerchr14:100914862..100929407hg17UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3814546
hg1914546
hg1814546
hg1714546
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517359
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668665
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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