A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511256



Internal ID22569208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122820763..122842473hg38UCSC Ensembl
chr9:125583042..125604752hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3821711
hg1921711
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864166
Supporting Variants
Samples
Known GenesPDCL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511256
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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