A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941124



Internal ID21361193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37280746..37280746hg38UCSC Ensembl
chr13:37854883..37854883hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194114
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941124
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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