A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661081



Internal ID9927186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154359877..154362020hg38UCSC Ensembl
chr6:154681011..154683154hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382144
hg192144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6015324, essv6056647, essv6587840
SamplesNA19437, NA19318, NA19316
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661081
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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