A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856713



Internal ID22631648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42107066..42120851hg38UCSC Ensembl
chr10:42602514..42616299hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3813786
hg1913786
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856713
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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