A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514755



Internal ID22572714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91649738..91652737hg38UCSC Ensembl
chr9:94412020..94415019hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848293
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514755
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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