A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419493



Internal ID21077046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90228450..90229053hg38UCSC Ensembl
chr8:91240678..91241281hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173701
Samples
Known GenesLINC00534
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419493
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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