A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075422



Internal ID21984655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174114362..174114362hg38UCSC Ensembl
chr5:173541365..173541365hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075422
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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