A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432879



Internal ID21394881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55536398..55539037hg38UCSC Ensembl
chr19:56047765..56050404hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382640
hg192640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753031
SamplesMDQ025
Known GenesSBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432879
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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