A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049770



Internal ID21959003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4974076..4976222hg38UCSC Ensembl
chr19:4974087..4976233hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382147
hg192147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619505
Samples
Known GenesKDM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049770
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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