A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732827



Internal ID20508753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4974045..4976189hg38UCSC Ensembl
chr19:4974056..4976200hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382145
hg192145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283608
Samples
Known GenesKDM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732827
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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