A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663992



Internal ID9930097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27190744..27192106hg38UCSC Ensembl
chr6:27158523..27159885hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381363
hg191363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5968539, essv6429706, essv5468367, essv5958923, essv5693613, essv5492154, essv6514377, essv6393124, essv6460934, essv6217902
SamplesNA12286, NA19819, NA18602, NA19404, NA19471, NA19391, HG00320, HG00580, NA18624, NA18623
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663992
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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