A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950702



Internal ID21370771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103768604..103768604hg38UCSC Ensembl
chr12:104162382..104162382hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193304
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950702
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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