A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191593



Internal ID20758633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10654617..10678090hg38UCSC Ensembl
chr17:10557934..10581407hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3823474
hg1923474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506362
Supporting Variants
Samples
Known GenesMYH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191593
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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