A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476719



Internal ID22534617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45230066..45242472hg38UCSC Ensembl
chr19:45733324..45745730hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3812407
hg1912407
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885036
Supporting Variants
Samples
Known GenesEXOC3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476719
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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