A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406058



Internal ID21063611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26202619..26216555hg38UCSC Ensembl
chr6:26202847..26216783hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3813937
hg1913937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140730
Samples
Known GenesHIST1H2BG, HIST1H4E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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