A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140259



Internal ID20707299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144007501..144008800hg38UCSC Ensembl
chr6:144328638..144329937hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605297
Supporting Variants
Samples
Known GenesHYMAI, PLAGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.05402


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