A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863744



Internal ID22638679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76571648..76577670hg38UCSC Ensembl
chr13:77145783..77151805hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg386023
hg196023
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455032, nssv17452110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863744
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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