A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419185



Internal ID21076738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94087577..94089651hg38UCSC Ensembl
chr8:95099805..95101879hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382075
hg192075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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