A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698382



Internal ID15435034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86584751..86605370hg38UCSC Ensembl
Innerchr14:87051095..87071714hg19UCSC Ensembl
Innerchr14:86120848..86141467hg18UCSC Ensembl
Innerchr14:86120848..86141467hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3820620
hg1920620
hg1820620
hg1720620
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522747
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698382
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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