A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211435



Internal ID20778475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173880377..174253847hg38UCSC Ensembl
chr3:173598167..173971637hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38373471
hg19373471
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355733
Supporting Variants
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211435
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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