A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661593



Internal ID9581012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157112341..157116537hg38UCSC Ensembl
chr4:158033493..158037689hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg384197
hg194197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6286791, essv5514762
SamplesHG01101, HG01356
Known GenesGLRB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661593
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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