A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058802



Internal ID21968035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38870016..38870016hg38UCSC Ensembl
chr1:39335688..39335688hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535035
Samples
Known GenesGJA9-MYCBP, MYCBP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058802
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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