A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388302



Internal ID21045855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:129343027..129349554hg38UCSC Ensembl
chr4:130264182..130270709hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg386528
hg196528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388302
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