A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077251



Internal ID21986484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177468042..177468042hg38UCSC Ensembl
chr5:176895043..176895043hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565789
Samples
Known GenesDBN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077251
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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