A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943419



Internal ID21363488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110043600..110043600hg38UCSC Ensembl
chr13:110695947..110695947hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194768
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943419
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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