A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5620273



Internal ID8597676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151869543..151873489hg38UCSC Ensembl
chr5:151249104..151253050hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383947
hg193947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677174
Supporting Variants
SamplesNA18498
Known GenesGLRA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5620273
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