A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5645413



Internal ID9463509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112101400..112103199hg38UCSC Ensembl
Outerchr6:112101363..112103249hg38UCSC Ensembl
Innerchr6:112422603..112424402hg19UCSC Ensembl
Outerchr6:112422566..112424452hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381887
hg191887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676434
Supporting Variants
SamplesNA18916
Known GenesFAM229B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5645413
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