A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937441



Internal ID21357510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103627840..103627840hg38UCSC Ensembl
chr5:102963541..102963541hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201030
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937441
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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