A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601052



Internal ID21793099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18267772..18268622hg38UCSC Ensembl
chrUn_gl000212:96524..97374hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022427
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601052
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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