A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362164



Internal ID21019717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28118988..28164518hg38UCSC Ensembl
chr4:28120610..28166140hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3845531
hg1945531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116278
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362164
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