A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432857



Internal ID21394859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54220029..54239661hg38UCSC Ensembl
chr19:54723893..54743537hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3819633
hg1919645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv377n172
Supporting Variantsnssv15753005
SamplesSMI034
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432857
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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