A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849178



Internal ID22624113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99254042..99264484hg38UCSC Ensembl
chr13:99906296..99916738hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3810443
hg1910443
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463257
Samples
Known GenesGPR18, MIR548AN, UBAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849178
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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