A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093880



Internal ID21286724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:14773349..14777850hg38UCSC Ensembl
Innerchr12:14926283..14930784hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg384502
hg194502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110976
Supporting Variants
Samplessample393
Known GenesH2AFJ
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093880
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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