A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051633



Internal ID21960866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11424528..11424689hg38UCSC Ensembl
chr19:11535197..11535360hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38162
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634948
Samples
Known GenesCCDC151
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051633
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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