A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042483



Internal ID21951799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37692531..37692631hg38UCSC Ensembl
chr19:38183432..38183532hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042483
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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