A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625137



Internal ID6665288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3217520..3339788hg38UCSC Ensembl
chr11:3238750..3361018hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38122269
hg19122269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv176e214
Supporting Variantsessv13993994, essv13993985, essv13994011, essv13993984, essv13993997, essv13993989, essv13993982, essv13994001, essv13994010, essv13994003, essv13994008, essv13993986, essv13994004, essv13994005, essv13993990, essv13994002, essv13994009, essv13993988, essv13993983, essv13993987, essv13994000, essv13994006, essv13993992, essv13993999, essv13994007, essv13993996, essv13993995, essv13993998, essv13993991, essv13993993
SamplesNA19028, HG03548, HG03052, NA19204, HG02852, HG02870, HG02323, HG03297, NA19119, HG02840, HG02505, NA19137, NA19456, HG01605, NA19913, HG02144, HG01941, HG02968, HG02537, HG03311, HG01956, HG02772, NA19019, HG01915, NA18865, HG03127, HG01342, HG03410, HG01914, NA19030
Known GenesMRGPRE, MRGPRG, MRGPRG-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625137
Frequency
Sample Size2504
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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