A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667963



Internal ID9934068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112323853..112324629hg38UCSC Ensembl
chr6:112645055..112645831hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38777
hg19777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5787405, essv6459337, essv5890152, essv5788564, essv5753234, essv6092209, essv6102626, essv5650991, essv5906334, essv6527933, essv6490830, essv6436363, essv5572902, essv6192179, essv6313452
SamplesNA19350, NA19359, NA19377, NA18870, NA19379, NA19130, NA19445, HG01183, NA19347, NA19453, NA19436, NA19380, NA19428, NA19713, NA18505
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667963
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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