A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633617



Internal ID21825664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61969618..61969669hg38UCSC Ensembl
chr18:59636851..59636902hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029089
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633617
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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