A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029800



Internal ID21939143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61241696..61244834hg38UCSC Ensembl
chr17:59319057..59322195hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg383139
hg193139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619542
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029800
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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