A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432770



Internal ID21394772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14621533..14623283hg38UCSC Ensembl
chr19:14732345..14734095hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381751
hg191751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753742
SamplesSMI018
Known GenesEMR3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432770
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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