A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520846



Internal ID15101453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103891739..103892784hg38UCSC Ensembl
Innerchr14:104358076..104359121hg19UCSC Ensembl
Innerchr14:103427829..103428874hg18UCSC Ensembl
Innerchr14:103427829..103428874hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381046
hg191046
hg181046
hg171046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676336, nssv677893
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520846
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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