A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433382



Internal ID21090935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98107915..98114435hg38UCSC Ensembl
chr8:99120143..99126663hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg386521
hg196521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173836
Samples
Known GenesHRSP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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