A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980592



Internal ID20547632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129945329..129948684hg38UCSC Ensembl
chr10:131743593..131746948hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383356
hg193356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450023
Supporting Variants
Samples
Known GenesEBF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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