A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862057



Internal ID22636992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103395665..103402281hg38UCSC Ensembl
chr13:104048015..104054631hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg386617
hg196617
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862057
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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