A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658372



Internal ID9924477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87941590..87941662hg38UCSC Ensembl
chr6:88651308..88651380hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5997276, essv5680647, essv6433893, essv5441076, essv6272122, essv5955583, essv5431331, essv6402679, essv6268211, essv5509477, essv6315319, essv5739272, essv5619707, essv5957991, essv5758926
SamplesNA11829, NA12751, NA12155, NA11992, NA19138, NA19238, NA19210, NA11894, NA19099, NA18858, NA19108, NA19240, NA07037, NA12006, NA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658372
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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