A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056501



Internal ID21965734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29920154..29920209hg38UCSC Ensembl
chr19:30411061..30411116hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056501
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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