A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511426



Internal ID22569378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128264196..128266790hg38UCSC Ensembl
chr9:131026475..131029069hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382595
hg192595
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856758
Supporting Variants
Samples
Known GenesGOLGA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511426
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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