A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929432



Internal ID22704686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113145373..113145430hg38UCSC Ensembl
chr13:113799687..113799744hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387282
Samples
Known GenesF10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929432
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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