A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375571



Internal ID21033124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170000060..170178407hg38UCSC Ensembl
chr3:169717848..169896195hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38178348
hg19178348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209202
Samples
Known GenesGPR160, PHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375571
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