A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953722



Internal ID21373791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105908615..105908615hg38UCSC Ensembl
chr7:105549061..105549061hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203681, nssv15203682
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953722
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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