A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421799



Internal ID21079352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:136844795..136989225hg38UCSC Ensembl
chr8:137857038..138001468hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38144431
hg19144431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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