A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265721



Internal ID20474939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60667364..60667364hg38UCSC Ensembl
chr5:59963191..59963191hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764756
Supporting Variants
Samples
Known GenesDEPDC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265721
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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