A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852416



Internal ID22627351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133078180..133107146hg38UCSC Ensembl
chr10:134891684..134920650hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3828967
hg1928967
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467107
Samples
Known GenesGPR123
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852416
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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