A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766470



Internal ID20542330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93550235..93550235hg38UCSC Ensembl
chr5:92885941..92885941hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287575
Samples
Known GenesNR2F1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766470
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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