A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023665



Internal ID21933008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110813079..110813253hg38UCSC Ensembl
chr13:111465426..111465600hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023665
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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