A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095585



Internal ID21276004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28628578..28632072hg38UCSC Ensembl
Innerchr14:29097784..29101278hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg383495
hg193495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112516
Supporting Variants
Samplessample231
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095585
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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