A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001119



Internal ID21910462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93618734..93618942hg38UCSC Ensembl
chr9:96381016..96381224hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593088
Samples
Known GenesPHF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001119
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