A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981661



Internal ID20548701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43602701..43606300hg38UCSC Ensembl
chr10:44098149..44101748hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448206
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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