A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430213



Internal ID22488083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107916656..107926166hg38UCSC Ensembl
chr9:110678937..110688447hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg389511
hg199511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907780
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430213
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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