A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686863



Internal ID15076829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106470101..106688061hg38UCSC Ensembl
Innerchr14:106926025..107144078hg19UCSC Ensembl
Innerchr14:105997070..106215123hg18UCSC Ensembl
Innerchr14:105997070..106215123hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38217961
hg19218054
hg18218054
hg17218054
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)nssv686863
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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