A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980450



Internal ID20547490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119717701..119720600hg38UCSC Ensembl
chr10:121477213..121480112hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442812
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980450
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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