A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860558



Internal ID22635493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87622848..87624087hg38UCSC Ensembl
chr13:88275103..88276342hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464153, nssv17467114
Samples
Known GenesMIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860558
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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