A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078692



Internal ID21987925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142076503..142076503hg38UCSC Ensembl
chr5:141456068..141456068hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552791
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078692
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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