A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856589



Internal ID22631524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5467531..5476451hg38UCSC Ensembl
chr10:5509494..5518414hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg388921
hg198921
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454909
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856589
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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