A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982632



Internal ID20549672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62220901..62221800hg38UCSC Ensembl
chr10:63980660..63981559hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438003
Supporting Variants
Samples
Known GenesRTKN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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