A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200936



Internal ID20767976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157763251..157763759hg38UCSC Ensembl
chr1:157733041..157733549hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333015
Supporting Variants
Samples
Known GenesFCRL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200936
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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