A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938102



Internal ID22713480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85267961..85276693hg38UCSC Ensembl
chr13:85842096..85850828hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg388733
hg198733
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938102
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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