A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420041



Internal ID21077594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133542515..133546787hg38UCSC Ensembl
chr8:134554758..134559030hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg384273
hg194273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164686
Samples
Known GenesST3GAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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