A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943860



Internal ID22719315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92037702..92239998hg38UCSC Ensembl
chr13:92689955..92892251hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38202297
hg19202297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386551
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943860
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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