A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514571



Internal ID22572529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87073090..87076322hg38UCSC Ensembl
chr9:89688005..89691237hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg383233
hg193233
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514571
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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