A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367071



Internal ID21024624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3883335..4150388hg38UCSC Ensembl
chr4:3885062..4152115hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38267054
hg19267054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5134n223
Supporting Variantsnssv18116040
Samples
Known GenesFAM86EP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367071
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