A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211403



Internal ID20778443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14946001..14949400hg38UCSC Ensembl
chr3:14987508..14990907hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367471
Supporting Variants
Samples
Known GenesFGD5-AS1, NR2C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211403
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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