A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978298



Internal ID20545338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117181255..117181620hg38UCSC Ensembl
chr10:118940766..118941131hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978298
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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