A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442999



Internal ID21100552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92446202..92450454hg38UCSC Ensembl
chr10:94205959..94210211hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg384253
hg194253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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