A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039185



Internal ID20606225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81605024..81605375hg38UCSC Ensembl
chr17:79572050..79572401hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522980
Supporting Variants
Samples
Known GenesNPLOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00538


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