A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451664



Internal ID22509536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25185189..25201932hg38UCSC Ensembl
chr10:25474118..25490861hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3816744
hg1916744
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848442
Supporting Variants
Samples
Known GenesGPR158
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451664
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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