A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060182



Internal ID21969415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30952162..30952246hg38UCSC Ensembl
chr19:31443068..31443152hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060182
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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