A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199748



Internal ID21338544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113453291..113453459hg38UCSC Ensembl
chr9:116215571..116215739hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954824
Supporting Variants
SamplesHG002
Known GenesRGS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199748
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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