A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864220



Internal ID22639155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26730577..26751146hg38UCSC Ensembl
chr13:27304714..27325283hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3820570
hg1920570
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864220
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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