A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851426



Internal ID22626361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20873822..20875699hg38UCSC Ensembl
chr10:21162751..21164628hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469198
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851426
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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