A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027054



Internal ID21936397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74732461..74733605hg38UCSC Ensembl
chr17:72728600..72729744hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381145
hg191145
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621416
Samples
Known GenesRAB37
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027054
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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