A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418761



Internal ID21076314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98065841..98068327hg38UCSC Ensembl
chr8:99078069..99080555hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg382487
hg192487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173832
Samples
Known GenesC8orf47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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