A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980598



Internal ID20547638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130055889..130103364hg38UCSC Ensembl
chr10:131854153..131901628hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3847476
hg1947476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444345
Supporting Variants
Samples
Known GenesLINC00959
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980598
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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