A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110976



Internal ID21294242
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 StatusM
Merged Variants
Supporting Variantsnssv14093880
Samplessample393
Known GenesH2AFJ
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110976
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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