A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686527



Internal ID15076493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106470101..106711347hg38UCSC Ensembl
Innerchr14:106926025..107166594hg19UCSC Ensembl
Innerchr14:105997070..106237639hg18UCSC Ensembl
Innerchr14:105997070..106237639hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38241247
hg19240570
hg18240570
hg17240570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known GenesLINC00221
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686527
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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