A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867004



Internal ID22641939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68543170..68544627hg38UCSC Ensembl
chr10:70302927..70304384hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867004
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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