A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393754



Internal ID21051307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38026925..38029478hg38UCSC Ensembl
chr5:38027027..38029580hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg382554
hg192554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393754
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