A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979114



Internal ID20546154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20628933..20629632hg38UCSC Ensembl
chr10:20917862..20918561hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979114
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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