A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652654



Internal ID15042620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106470101..106779068hg38UCSC Ensembl
Innerchr14:106926025..107187307hg19UCSC Ensembl
Innerchr14:105997070..106258352hg18UCSC Ensembl
Innerchr14:105997070..106258352hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38308968
hg19261283
hg18261283
hg17261283
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)nssv652654
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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