A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851276



Internal ID22626211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58708674..58728711hg38UCSC Ensembl
chr10:60468434..60488471hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3820038
hg1920038
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453704
Samples
Known GenesBICC1, FAM133CP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851276
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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