A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703550



Internal ID15093516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106561191..106631857hg38UCSC Ensembl
Innerchr14:107017181..107087862hg19UCSC Ensembl
Innerchr14:106088226..106158907hg18UCSC Ensembl
Innerchr14:106088226..106158907hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3870667
hg1970682
hg1870682
hg1770682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703550
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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