A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626303



Internal ID21818350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31525321..31525947hg38UCSC Ensembl
chr18:29105284..29105910hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029363
Supporting Variants
Samples
Known GenesDSG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626303
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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