A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853166



Internal ID22628101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69262127..69270819hg38UCSC Ensembl
chr13:69836259..69844951hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg388693
hg198693
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853166
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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