A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940385



Internal ID21360454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79419091..79419160hg38UCSC Ensembl
chr13:79993226..79993295hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15182417
SamplesHG002
Known GenesRBM26-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940385
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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