A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518090



Internal ID15445383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35333277..35371035hg38UCSC Ensembl
Innerchr14:35802483..35840241hg19UCSC Ensembl
Innerchr14:34872234..34909992hg18UCSC Ensembl
Innerchr14:34872234..34909992hg17UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3837759
hg1937759
hg1837759
hg1737759
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656204, nssv663816, nssv674743, nssv685661, nssv676846, nssv679493, nssv682258, nssv698473, nssv684687, nssv672759
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518090
Frequency
Sample Size2026
Observed Gain1
Observed Loss9
Observed Complex0
Frequencyn/a


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