A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450863



Internal ID21108416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:799257..808649hg38UCSC Ensembl
chr10:845197..854589hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg389393
hg199393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984406
Samples
Known GenesLARP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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