A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929042



Internal ID21349113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32397296..32397296hg38UCSC Ensembl
chr3:32438788..32438788hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189694
SamplesHG002
Known GenesCMTM7
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929042
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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