A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767932



Internal ID20543792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6313737..6313737hg38UCSC Ensembl
chr5:6313850..6313850hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264756
Samples
Known GenesFLJ33360
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767932
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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