A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392431



Internal ID21049984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169340659..169342305hg38UCSC Ensembl
chr4:170261810..170263456hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg381647
hg191647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392431
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