A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446270



Internal ID22504140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113384381..113385400hg38UCSC Ensembl
chr9:116146661..116147680hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381020
hg191020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917074
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446270
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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