A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435492



Internal ID22493362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88190911..88191473hg38UCSC Ensembl
chr9:90805826..90806388hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912387
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435492
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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