A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069012



Internal ID20636052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49703182..49706197hg38UCSC Ensembl
chr20:48319719..48322734hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg383016
hg193016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550868
Supporting Variants
Samples
Known GenesB4GALT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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