A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624109



Internal ID21816156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57265219..57266252hg38UCSC Ensembl
chr19:57776587..57777620hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381034
hg191034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042376
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624109
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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