A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096935



Internal ID21283712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73057623..73061923hg38UCSC Ensembl
Innerchr13:73631761..73636061hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg384301
hg194301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114462
Supporting Variants
Samplessample349
Known GenesKLF5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096935
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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