A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432816



Internal ID21394818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34390096..34393095hg38UCSC Ensembl
chr19:34881001..34884000hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752010
SamplesBTQ038
Known GenesGPI
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432816
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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