A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860585



Internal ID22635520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32487550..32496776hg38UCSC Ensembl
chr13:33061687..33070913hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg389227
hg199227
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452889
Samples
Known GenesMINOS1P1, N4BP2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860585
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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