A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512213



Internal ID22570165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20924700..20936968hg38UCSC Ensembl
chr9:20924699..20936967hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3812269
hg1912269
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862036
Supporting Variants
Samples
Known GenesFOCAD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512213
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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