A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932651



Internal ID21352720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105969154..105969154hg38UCSC Ensembl
chr2:106585610..106585610hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187881
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932651
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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