A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435497



Internal ID22493367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105108006..105110582hg38UCSC Ensembl
chr9:107870287..107872863hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382577
hg192577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435497
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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