A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395481



Internal ID22453351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45229188..45229312hg38UCSC Ensembl
chr19:45732446..45732570hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927590
Supporting Variants
Samples
Known GenesEXOC3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395481
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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