A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679043



Internal ID15069009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106470101..106690675hg38UCSC Ensembl
Innerchr14:106926025..107146692hg19UCSC Ensembl
Innerchr14:105997070..106217737hg18UCSC Ensembl
Innerchr14:105997070..106217737hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38220575
hg19220668
hg18220668
hg17220668
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)nssv679043
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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