A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368062



Internal ID21025615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173527901..173651700hg38UCSC Ensembl
chr3:173245691..173369490hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38123800
hg19123800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5091n223
Supporting Variantsnssv18098878
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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