A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270517



Internal ID20479735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38870019..38870019hg38UCSC Ensembl
chr1:39335691..39335691hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760532
Supporting Variants
Samples
Known GenesGJA9-MYCBP, MYCBP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270517
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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