A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6574717



Internal ID9782451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188015036..188016974hg38UCSC Ensembl
chr3:187732824..187734762hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381939
hg191939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674966
Supporting Variants
SamplesNA19771
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6574717
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