A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432337



Internal ID21394339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30668059..30669208hg38UCSC Ensembl
chr16:30679380..30680529hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381150
hg191150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753384
SamplesBTQ055
Known GenesFBRS
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432337
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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