A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111169



Internal ID22020402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53945606..53945606hg38UCSC Ensembl
chr20:52562145..52562145hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg382730
hg192730
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621440
Samples
Known GenesBCAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111169
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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