A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467107



Internal ID22524999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133078180..133107146hg38UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38n/a
hg1928967
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variants
Supporting Variants
Samples
Known GenesGPR123
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467107
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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