A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068999



Internal ID20636039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49529188..49619491hg38UCSC Ensembl
chr20:48145725..48236028hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3890304
hg1990304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551242
Supporting Variants
Samples
Known GenesPTGIS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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