A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865064



Internal ID22639999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48106188..48108365hg38UCSC Ensembl
chr13:48680324..48682501hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg382178
hg192178
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459147, nssv17466782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865064
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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