A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368911



Internal ID21026464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119436632..119437237hg38UCSC Ensembl
chr3:119155479..119156084hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094554
Samples
Known GenesTMEM39A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368911
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