A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438290



Internal ID21095843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84045469..84045831hg38UCSC Ensembl
chr10:85805225..85805587hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438290
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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