A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830594



Internal ID22605529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114735696..114781095hg38UCSC Ensembl
chr2:115493273..115538672hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3845400
hg1945400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485753
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830594
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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