A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688925



Internal ID15078891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106470101..106666909hg38UCSC Ensembl
Innerchr14:106926025..107122925hg19UCSC Ensembl
Innerchr14:105997070..106193970hg18UCSC Ensembl
Innerchr14:105997070..106193970hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38196809
hg19196901
hg18196901
hg17196901
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)nssv688925
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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