A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981185



Internal ID20548225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26620053..26695016hg38UCSC Ensembl
chr10:26908982..26983945hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3874964
hg1974964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450410
Supporting Variants
Samples
Known GenesLINC00202-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00025


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