A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062288



Internal ID21971521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170278497..170278497hg38UCSC Ensembl
chr5:169705501..169705501hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560630
Samples
Known GenesLCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062288
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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