A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5741013



Internal ID8718416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59581052..59584964hg38UCSC Ensembl
chr1:60046724..60050636hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg383913
hg193913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675145
Supporting Variants
SamplesNA19379
Known GenesFGGY
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5741013
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