A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979455



Internal ID20546495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109347276..109348074hg38UCSC Ensembl
chr10:111107034..111107832hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438688
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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