A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193231



Internal ID20760271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25654319..25738978hg38UCSC Ensembl
chr10:25943248..26027907hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3884660
hg1984660
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444156
Supporting Variants
Samples
Known GenesLINC00836
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193231
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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