A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486587



Internal ID22544502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16279462..16280461hg38UCSC Ensembl
chr3:16320969..16321968hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835033
Supporting Variants
Samples
Known GenesOXNAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486587
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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