A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867115



Internal ID22642050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38363431..38364534hg38UCSC Ensembl
chr13:38937568..38938671hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467984, nssv17454926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867115
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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