A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855849



Internal ID22630784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102043695..102050277hg38UCSC Ensembl
chr13:102696045..102702627hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg386583
hg196583
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450288
Samples
Known GenesFGF14, MIR4705
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855849
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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