A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848130



Internal ID22623065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88225612..88249627hg38UCSC Ensembl
chr13:88877867..88901882hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3824016
hg1924016
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848130
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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