A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134697



Internal ID20701737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105254928..105276116hg38UCSC Ensembl
chr6:105702803..105723991hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3821189
hg1921189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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