A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448215



Internal ID21105768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84291949..84294443hg38UCSC Ensembl
chr10:86051705..86054199hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg382495
hg192495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984591
Samples
Known GenesLINC00858
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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