A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669364



Internal ID9935469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27029453..27030046hg38UCSC Ensembl
chr6:26997232..26997825hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6194007, essv6223698, essv5679616, essv6353277, essv6065135, essv6057270, essv6087487, essv6220302, essv5619456, essv5573385
SamplesNA19397, HG01359, HG01052, HG01188, NA19377, NA18870, NA19396, NA19917, NA19625, HG00554
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669364
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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