A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023758



Internal ID21933101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:538035..538101hg38UCSC Ensembl
chr19:538035..538101hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626775
Samples
Known GenesCDC34
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023758
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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