A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043712



Internal ID21953006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34028233..34028323hg38UCSC Ensembl
chr19:34519138..34519228hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043712
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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