A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049045



Internal ID20616085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4974078..4976207hg38UCSC Ensembl
chr19:4974089..4976218hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382130
hg192130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523999
Supporting Variants
Samples
Known GenesKDM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049045
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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