A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985397



Internal ID20552437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92194832..92200267hg38UCSC Ensembl
chr10:93954589..93960024hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg385436
hg195436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449415
Supporting Variants
Samples
Known GenesCPEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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