A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984853



Internal ID20551894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88265701..88297800hg38UCSC Ensembl
chr10:90025458..90057557hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3832100
hg1932100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454782
Supporting Variants
Samples
Known GenesRNLS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984853
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00066


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