A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953755



Internal ID21373824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101680713..101680713hg38UCSC Ensembl
chr3:101399557..101399557hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188423
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953755
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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