A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737782



Internal ID20513745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35105898..35106181hg38UCSC Ensembl
chr19:35596802..35597085hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265701
Samples
Known GenesHPN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737782
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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