A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138742



Internal ID20705782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126344165..126344533hg38UCSC Ensembl
chr6:126665311..126665679hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619602
Supporting Variants
Samples
Known GenesCENPW
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138742
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00145


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