A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038017



Internal ID20605057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71551516..71571593hg38UCSC Ensembl
chr17:69547657..69567734hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3820078
hg1920078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524653
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00046


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