A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672782



Internal ID15062748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106489875..106649040hg38UCSC Ensembl
Innerchr14:106945882..107105043hg19UCSC Ensembl
Innerchr14:106016927..106176088hg18UCSC Ensembl
Innerchr14:106016927..106176088hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38159166
hg19159162
hg18159162
hg17159162
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)nssv672782
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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