A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144233



Internal ID20711273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46540349..46544366hg38UCSC Ensembl
chr6:46508086..46512103hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg384018
hg194018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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