A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510801



Internal ID22568752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112208472..112210521hg38UCSC Ensembl
chr9:114970752..114972801hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382050
hg192050
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861761
Supporting Variants
Samples
Known GenesMIR3134
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510801
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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