A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513568



Internal ID22571523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43020906..43034056hg38UCSC Ensembl
chr9:42949208..42962341hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3813151
hg1913134
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513568
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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