A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982091



Internal ID20549131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52361888..52370910hg38UCSC Ensembl
chr10:54121648..54130670hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg389023
hg199023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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