A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857250



Internal ID22632185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76560073..76602559hg38UCSC Ensembl
chr13:77134208..77176694hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3842487
hg1942487
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857250
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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