A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135482



Internal ID20702522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112651839..112652432hg38UCSC Ensembl
chr6:112973041..112973634hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618596
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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