A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514564



Internal ID22572522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87044044..87063292hg38UCSC Ensembl
chr9:89658959..89678207hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3819249
hg1919249
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514564
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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