A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848678



Internal ID22623613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98317738..98326053hg38UCSC Ensembl
chr13:98969992..98978307hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg388316
hg198316
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462146
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848678
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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