A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626578



Internal ID21818625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44897007..44897089hg38UCSC Ensembl
chr19:45400264..45400346hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053034
Supporting Variants
Samples
Known GenesTOMM40
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626578
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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