A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944980



Internal ID21365049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32453171..32453171hg38UCSC Ensembl
chr12:32606105..32606105hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193950
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944980
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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