A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404145



Internal ID21061698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81992189..81992603hg38UCSC Ensembl
chr5:81288008..81288422hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132943
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404145
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