A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212765



Internal ID20779805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17445966..17541248hg38UCSC Ensembl
chr4:17447589..17542871hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3895283
hg1995283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357703
Supporting Variants
Samples
Known GenesCLRN2, QDPR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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