A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985796



Internal ID20552836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98427806..98428695hg38UCSC Ensembl
chr10:100187563..100188452hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449334
Supporting Variants
Samples
Known GenesHPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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