A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387360



Internal ID21044913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43468894..43472453hg38UCSC Ensembl
chr4:43470911..43474470hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg383560
hg193560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387360
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