A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360186



Internal ID21017739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181107441..181111492hg38UCSC Ensembl
chr3:180825229..180829280hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg384052
hg194052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097759
Samples
Known GenesSOX2-OT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360186
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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