A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663135



Internal ID9582554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:236689..236894hg38UCSC Ensembl
chr3:278372..278577hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6181677, essv6568506, essv6246957, essv6272039, essv6433626, essv5842294, essv6218027, essv5999643, essv6415106, essv6220047, essv6328634, essv6461255, essv6132426, essv6207232, essv5681057, essv5807843, essv6133325, essv5422195, essv6340568, essv6352854, essv5611207, essv6331186, essv6012747
SamplesNA18861, NA19436, NA18871, NA19311, NA18517, NA19920, NA18489, NA19461, NA18488, NA18873, NA19390, NA19197, NA19190, NA19360, NA19377, NA19189, NA18486, NA20344, NA19713, NA18858, NA20332, NA18908, NA18519
Known GenesCHL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663135
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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