A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936737



Internal ID21356806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65609984..65609984hg38UCSC Ensembl
chr3:65595659..65595659hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189254
SamplesHG002
Known GenesMAGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936737
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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