A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861112



Internal ID22636047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85268401..85272747hg38UCSC Ensembl
chr13:85842536..85846882hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg384347
hg194347
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861112
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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