A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939049



Internal ID21359118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87492124..87492124hg38UCSC Ensembl
chr13:88144379..88144379hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193542
SamplesHG002
Known GenesMIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939049
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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