A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980531



Internal ID20547571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121125318..121127025hg38UCSC Ensembl
chr10:122884832..122886539hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg381708
hg191708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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