A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386758



Internal ID21044311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169011466..169015846hg38UCSC Ensembl
chr4:169932617..169936997hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg384381
hg194381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386758
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