A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675572



Internal ID9941677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63420995..63437452hg38UCSC Ensembl
chr11:63188467..63204924hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3816458
hg1916458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5727313, essv6334907, essv6188302, essv6469748, essv5795608
SamplesNA19384, HG01133, HG01124, NA19434, NA19360
Known GenesMIR3680-1, MIR3680-2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675572
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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