A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432113



Internal ID21394115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51911691..51912301hg38UCSC Ensembl
chr14:52378409..52379019hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15746781
SamplesMDQ045
Known GenesGNG2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432113
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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