A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021770



Internal ID21931113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32529914..32532772hg38UCSC Ensembl
chr13:33104051..33106909hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg382859
hg192859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611520
Samples
Known GenesN4BP2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021770
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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