A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164254



Internal ID20731294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120673457..120922249hg38UCSC Ensembl
chr8:121685697..121934489hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38248793
hg19248793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416355
Supporting Variants
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164254
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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