A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985384



Internal ID20552424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91973206..91975496hg38UCSC Ensembl
chr10:93732963..93735253hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg382291
hg192291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443958
Supporting Variants
Samples
Known GenesBTAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985384
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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