A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164252



Internal ID20731292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120637984..120644776hg38UCSC Ensembl
chr8:121650224..121657016hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg386793
hg196793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425454
Supporting Variants
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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