A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618378



Internal ID20991449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138735469..138738212hg38UCSC Ensembl
chr6:139056606..139059349hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg382744
hg192744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138402
Samples
Known GenesLOC100507462
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618378
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