A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041234



Internal ID21950570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12020773..12020890hg38UCSC Ensembl
chr19:12131588..12131705hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625339
Samples
Known GenesZNF433
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041234
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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