A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671532



Internal ID9937637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23412219..23419418hg38UCSC Ensembl
chr10:23701148..23708347hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6020507, essv6248396, essv6120867, essv5984433, essv6202567, essv5575663, essv6031374, essv5501441, essv5569810, essv6172741, essv6472160, essv5897023
SamplesNA19397, NA18861, NA19377, NA18870, NA19446, NA19396, NA19904, NA19383, NA19456, NA19452, HG01551, NA19435
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671532
Frequency
Sample Size1151
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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