A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432886



Internal ID21394888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7449115..7451114hg38UCSC Ensembl
chr19:7514001..7516000hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15746136
SamplesBTQ038
Known GenesARHGEF18
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432886
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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