A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954199



Internal ID21374269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118042421..118042421hg38UCSC Ensembl
chr2:118799997..118799997hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187576
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954199
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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