A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662175



Internal ID9581594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151192995..151197033hg38UCSC Ensembl
chr6:151514130..151518168hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384039
hg194039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5625669
SamplesNA18950
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662175
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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