A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606534



Internal ID20979605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144133981..144138241hg38UCSC Ensembl
chr6:144455118..144459378hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384261
hg194261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606534
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