A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077434



Internal ID21986667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14303565..14303565hg38UCSC Ensembl
chr5:14303674..14303674hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540582
Samples
Known GenesTRIO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077434
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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