A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052785



Internal ID21962018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18319442..18320544hg38UCSC Ensembl
chr19:18430252..18431354hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381103
hg191103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632462
Samples
Known GenesLSM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052785
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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