A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631291



Internal ID21823338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61176646..61176709hg38UCSC Ensembl
chr17:59254007..59254070hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029787
Supporting Variants
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631291
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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