A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091635



Internal ID21292422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27941109..27951643hg38UCSC Ensembl
Innerchr12:28094042..28104576hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3810535
hg1910535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118203
Supporting Variants
Samplessample88
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091635
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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