A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424273



Internal ID21081826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80077010..80091338hg38UCSC Ensembl
chr8:80989245..81003573hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3814329
hg1914329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171242
Samples
Known GenesTPD52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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