A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264756



Internal ID20473974
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 StatusS
Merged Variantsnsv4767932
Supporting Variants
Samples
Known GenesFLJ33360
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264756
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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