A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095822



Internal ID21278619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110652133..110660694hg38UCSC Ensembl
Innerchr13:111304480..111313041hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg388562
hg198562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111331
Supporting Variants
Samplessample271
Known GenesCARS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095822
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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