A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929811



Internal ID21349881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190690012..190690012hg38UCSC Ensembl
chr2:191554738..191554738hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186204
SamplesHG002
Known GenesNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929811
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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