A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140976



Internal ID20708016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145823348..145827725hg38UCSC Ensembl
chr6:146144484..146148861hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg384378
hg194378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609846
Supporting Variants
Samples
Known GenesLOC100507557
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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