A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049951



Internal ID20616991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6143473..6145066hg38UCSC Ensembl
chr19:6143484..6145077hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381594
hg191594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523195
Supporting Variants
Samples
Known GenesACSBG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049951
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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