A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103496



Internal ID21277304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:168112271..168115599hg38UCSC Ensembl
Innerchr3:167830059..167833387hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg383329
hg193329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111823
Supporting Variants
Samplessample25
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103496
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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