A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096664



Internal ID21269193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110673366..110676698hg38UCSC Ensembl
Innerchr1:111215988..111219320hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg383333
hg193333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116925
Supporting Variants
Samplessample136
Known GenesKCNA3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096664
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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