A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853590



Internal ID22628525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45972971..45975251hg38UCSC Ensembl
chr10:51620585..51622868hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382281
hg192284
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459883
Samples
Known GenesTIMM23
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853590
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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