A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978983



Internal ID20546023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17525801..17532160hg38UCSC Ensembl
chr10:17567800..17574159hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg386360
hg196360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441999
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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