A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513768



Internal ID22571724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60885015..60889550hg38UCSC Ensembl
chr9:41471287..41475822hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg384536
hg194536
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859108
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513768
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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