A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661273



Internal ID9927378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157925242..157925967hg38UCSC Ensembl
chr6:158346274..158346999hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5798302, essv5420242, essv5927632, essv5829438, essv5838625, essv5471948, essv6131400, essv5745532, essv5912136, essv5600833, essv5903552, essv5998741, essv5597272
SamplesNA18508, NA19350, NA18526, NA19448, NA19130, NA19908, NA19453, NA19338, NA18523, NA18945, NA19321, NA19434, NA19444
Known GenesSNX9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661273
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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