A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849814



Internal ID22624749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50870553..50872193hg38UCSC Ensembl
chr13:51444689..51446329hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381641
hg191641
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv529n209
Supporting Variantsnssv17460084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849814
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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