A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441269



Internal ID22499139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11449783..11718852hg38UCSC Ensembl
chr9:11449783..11718852hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38269070
hg19269070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919448
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441269
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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