A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057954



Internal ID21967187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38297040..38297646hg38UCSC Ensembl
chr19:38787680..38788286hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057954
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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