A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512167



Internal ID22570119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19706781..19708982hg38UCSC Ensembl
chr9:19706779..19708980hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg382202
hg192202
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860091
Supporting Variants
Samples
Known GenesSLC24A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512167
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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