A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076485



Internal ID21985718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109353503..109353503hg38UCSC Ensembl
chr5:108689204..108689204hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555876
Samples
Known GenesPJA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076485
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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