A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108631



Internal ID21285179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163139554..163228010hg38UCSC Ensembl
Innerchr3:162857342..162945798hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3888457
hg1988457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116170
Supporting Variants
Samplessample370
Known GenesCT64
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108631
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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