A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036326



Internal ID20603366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58792771..58816118hg38UCSC Ensembl
chr17:56870132..56893479hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3823348
hg1923348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526348
Supporting Variants
Samples
Known GenesPPM1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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