A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432839



Internal ID21394841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47992520..48083392hg38UCSC Ensembl
chr19:48495777..48586649hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3890873
hg1990873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv373n172
Supporting Variantsnssv15748863
SamplesNB11
Known GenesCABP5, ELSPBP1, PLA2G4C
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432839
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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