A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505450



Internal ID20878720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98646901..98652100hg38UCSC Ensembl
chr15:99190130..99195329hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2645n223
Supporting Variantsnssv18183548
Samples
Known GenesIGF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505450
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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