A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077126



Internal ID21986359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152257419..152257419hg38UCSC Ensembl
chr5:151636980..151636980hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381513
hg191513
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077126
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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