A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093692



Internal ID21282797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30084859..30090610hg38UCSC Ensembl
Innerchr12:30237792..30243543hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg385752
hg195752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113482
Supporting Variants
Samplessample331
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093692
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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