A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5691283



Internal ID8668686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155673048..155677151hg38UCSC Ensembl
chr4:156594200..156598303hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg384104
hg194104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674234
Supporting Variants
SamplesNA19452
Known GenesGUCY1A3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5691283
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