A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611786



Internal ID21803833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113841478..113841478hg38UCSC Ensembl
chr13:114544451..114544451hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097537
Supporting Variants
Samples
Known GenesGAS6, GAS6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611786
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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