A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700941



Internal ID21222782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93671158..93671369hg38UCSC Ensembl
chr9:96433440..96433651hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820024
Supporting Variants
Samples
Known GenesPHF2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700941
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.125


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