A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048378



Internal ID21957611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29514519..29514582hg38UCSC Ensembl
chr19:30005426..30005489hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626861
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048378
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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