A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5482491



Internal ID8459894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149668117..149674273hg38UCSC Ensembl
chr6:149989253..149995409hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg386157
hg196157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671976
Supporting Variants
SamplesNA19390
Known GenesLATS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5482491
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer