A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535035



Internal ID21859390
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 StatusS
Merged Variantsnsv6058802
Supporting Variants
Samples
Known GenesGJA9-MYCBP, MYCBP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535035
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer