A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669105



Internal ID9935210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26390725..26402931hg38UCSC Ensembl
Outerchr3:26390354..26403301hg38UCSC Ensembl
Innerchr3:26432216..26444422hg19UCSC Ensembl
Outerchr3:26431845..26444792hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3812948
hg1912948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5482343, essv6552889, essv6543468, essv6547335, essv6516388, essv6364080, essv5418297, essv5880462, essv6555385, essv5512644, essv6498632, essv5771808, essv5691266, essv6336382, essv5805937, essv5718655, essv6473595, essv6212770, essv5424064, essv6230486
SamplesNA11830, NA10851, NA12273, NA11933, NA11931, NA12004, NA07357, NA12341, NA07346, NA11918, NA12156, NA12044, NA12889, NA12342, NA11881, NA07051, NA12763, NA12347, NA12830, NA07000
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669105
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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