A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984591



Internal ID20551631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84291949..84294443hg38UCSC Ensembl
chr10:86051705..86054199hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg382495
hg192495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448215
Supporting Variants
Samples
Known GenesLINC00858
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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