A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432811



Internal ID21394813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31193095..31211094hg38UCSC Ensembl
chr19:31684001..31702000hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3818000
hg1918000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv370n172
Supporting Variantsnssv15752361, nssv15748061, nssv15746830
SamplesBTQ038, BTQ055, BTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432811
Frequency
Sample Size15
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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