A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739382



Internal ID20515355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34132664..34132839hg38UCSC Ensembl
chr19:34623569..34623744hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739382
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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