A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979001



Internal ID20546041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17794202..17796267hg38UCSC Ensembl
chr10:17836201..17838266hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg382066
hg192066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448404
Supporting Variants
Samples
Known GenesTMEM236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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