A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619659



Internal ID21811706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6507053..6509015hg38UCSC Ensembl
chr19:6507064..6509026hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381963
hg191963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619659
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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