A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983889



Internal ID20550929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74079801..74080700hg38UCSC Ensembl
chr10:75839559..75840458hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452310
Supporting Variants
Samples
Known GenesVCL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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