A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178368



Internal ID20745408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58706156..58712548hg38UCSC Ensembl
chr17:56783517..56789909hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg386393
hg196393
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528554
Supporting Variants
Samples
Known GenesRAD51C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178368
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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