A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981554



Internal ID20548594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51279314..51282293hg38UCSC Ensembl
chr10:53039074..53042053hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382980
hg192980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439823
Supporting Variants
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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