A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449031



Internal ID22506901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93964703..93966213hg38UCSC Ensembl
chr9:96726985..96728495hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381511
hg191511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920286
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449031
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