A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850920



Internal ID22625855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71871096..71875840hg38UCSC Ensembl
chr10:73630854..73635598hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384745
hg194745
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461323
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850920
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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