A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422978



Internal ID21080531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23191713..23208951hg38UCSC Ensembl
chr8:23049226..23066464hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3817239
hg1917239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167125
Samples
Known GenesTNFRSF10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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