A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934434



Internal ID22709760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33558662..33564774hg38UCSC Ensembl
chr13:34132799..34138911hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg386113
hg196113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372734
Samples
Known GenesSTARD13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934434
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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