A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513497



Internal ID22571452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42843902..42846925hg38UCSC Ensembl
chr9:44124194..44127217hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg383024
hg193024
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856761
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513497
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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