A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977657



Internal ID20544697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113448901..113457100hg38UCSC Ensembl
chr10:115208660..115216859hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446303
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00403


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