A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861096



Internal ID22636031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48574364..48578349hg38UCSC Ensembl
chr13:49148500..49152485hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg383986
hg193986
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463927
Samples
Known GenesLINC00462
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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