A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938001



Internal ID21358070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191742046..191742046hg38UCSC Ensembl
chr2:192606772..192606772hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186208
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938001
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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