A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368505



Internal ID21026058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16515820..16560633hg38UCSC Ensembl
chr4:16517443..16562256hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3844814
hg1944814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112073
Samples
Known GenesLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368505
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