A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936164



Internal ID21356234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26333430..26333430hg38UCSC Ensembl
chr2:26556298..26556298hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187817
SamplesHG002
Known GenesGPR113
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936164
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer