A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934454



Internal ID21354524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65342188..65342188hg38UCSC Ensembl
chr2:65569322..65569322hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187172
SamplesHG002
Known GenesSPRED2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934454
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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