A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749103



Internal ID21388248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73109850..73111849hg38UCSC Ensembl
chr3:73159001..73161000hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434086
Supporting Variants
SamplesNB07
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749103
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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