A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856525



Internal ID22631460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122712606..122723305hg38UCSC Ensembl
chr10:124472122..124482821hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856525
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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