A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387899



Internal ID21045452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83640993..83644559hg38UCSC Ensembl
chr4:84562146..84565712hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg383567
hg193567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387899
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