A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597974



Internal ID21790018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73575285..73575386hg38UCSC Ensembl
chr13:74149422..74149523hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597974
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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