A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060612



Internal ID21969845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54313010..54313010hg38UCSC Ensembl
chr5:53608840..53608840hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060612
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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