A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380985



Internal ID21038538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39945313..39967721hg38UCSC Ensembl
chr4:39946933..39969341hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3822409
hg1922409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117063
Samples
Known GenesPDS5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380985
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