A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381089



Internal ID21038642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96284331..96391401hg38UCSC Ensembl
chr4:97205482..97312552hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38107071
hg19107071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121972
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381089
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