A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741138



Internal ID20517115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29920149..29920209hg38UCSC Ensembl
chr19:30411056..30411116hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741138
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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