A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048646



Internal ID20615686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45229188..45229313hg38UCSC Ensembl
chr19:45732446..45732571hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528379
Supporting Variants
Samples
Known GenesEXOC3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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