A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658362



Internal ID15048328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106489875..106520946hg38UCSC Ensembl
Innerchr14:106945882..106976874hg19UCSC Ensembl
Innerchr14:106016927..106047919hg18UCSC Ensembl
Innerchr14:106016927..106047919hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3831072
hg1930993
hg1830993
hg1730993
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)nssv658362
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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