A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926036



Internal ID21346107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79624943..79624943hg38UCSC Ensembl
chr13:80199078..80199078hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192983
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926036
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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