A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432297



Internal ID21394299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13068144..13070143hg38UCSC Ensembl
chr16:13162001..13164000hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754333, nssv15748912
SamplesMDQ010, MDQ025
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432297
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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