A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489736



Internal ID22547656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181349734..181351724hg38UCSC Ensembl
chr3:181067522..181069512hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381991
hg191991
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835421
Supporting Variants
Samples
Known GenesSOX2-OT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489736
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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