A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980600



Internal ID20547640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130064900..130065278hg38UCSC Ensembl
chr10:131863164..131863542hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446533
Supporting Variants
Samples
Known GenesLINC00959
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00178


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