A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048454



Internal ID21957687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30384209..30384354hg38UCSC Ensembl
chr19:30875116..30875261hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618113
Samples
Known GenesZNF536
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048454
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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