A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850864



Internal ID22625799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27934203..27954352hg38UCSC Ensembl
chr13:28508340..28528489hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3820150
hg1920150
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451051
Samples
Known GenesATP5EP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850864
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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