A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6226119



Internal ID9915213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119456016..119491940hg38UCSC Ensembl
chr1:119998639..120034563hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3835925
hg1935925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677771
Supporting Variants
SamplesNA20812
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6226119
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