A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983065



Internal ID20550105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69325800..69325966hg38UCSC Ensembl
chr10:71085556..71085722hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449698
Supporting Variants
Samples
Known GenesHK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983065
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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