A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424028



Internal ID21081581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:99672975..99673712hg38UCSC Ensembl
chr8:100685203..100685940hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171897
Samples
Known GenesVPS13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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