A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512685



Internal ID22570639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29122111..29131619hg38UCSC Ensembl
chr9:29122109..29131617hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg389509
hg199509
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867474
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512685
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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