A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977252



Internal ID20544293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102215501..102217100hg38UCSC Ensembl
chr10:103975258..103976857hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439986
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00072


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