A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359652



Internal ID21017205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44898268..44901177hg38UCSC Ensembl
chr3:44939760..44942669hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382910
hg192910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100623
Samples
Known GenesTGM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359652
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