A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985996



Internal ID20553036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97406795..97408429hg38UCSC Ensembl
chr10:99166552..99168186hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381635
hg191635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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