A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385602



Internal ID21043155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134515652..134628146hg38UCSC Ensembl
chr4:135436807..135549301hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38112495
hg19112495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385602
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