A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866800



Internal ID22641735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58293089..58318861hg38UCSC Ensembl
chr10:60052849..60078621hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3825773
hg1925773
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866800
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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