A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063452



Internal ID21972685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16464186..16464186hg38UCSC Ensembl
chr5:16464295..16464295hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386084
hg196084
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548538
Samples
Known GenesZNF622
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063452
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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