A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420594



Internal ID21078147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54156139..54157378hg38UCSC Ensembl
chr8:55068699..55069938hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420594
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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