A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630047



Internal ID21822094
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 Variantsnsv6055033
Supporting Variants
Samples
Known GenesEXOC3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630047
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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