A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036282



Internal ID20603322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5797363..5804449hg38UCSC Ensembl
chr17:5700683..5707769hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg387087
hg197087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508615
Supporting Variants
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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