A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165703



Internal ID20732743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132642817..132643336hg38UCSC Ensembl
chr8:133655063..133655582hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422231
Supporting Variants
Samples
Known GenesLRRC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165703
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00081


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