A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985030



Internal ID20552070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90293379..90303193hg38UCSC Ensembl
chr10:92053136..92062950hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg389815
hg199815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985030
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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