A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672420



Internal ID9591839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28143578..28143877hg38UCSC Ensembl
chr10:28432507..28432806hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6381881, essv6230973, essv5598453, essv5889338, essv6015477, essv5983082, essv5868711, essv5784273, essv6474268, essv6593209, essv6001108, essv5821347, essv6086553, essv6273914, essv6098050, essv5548122, essv6036896, essv6558161, essv5552446, essv5455416, essv6473262, essv5664650, essv6428517, essv5616135, essv5598008, essv5398861, essv5834652, essv6164904, essv6498823, essv5440236, essv5932682, essv5993450, essv5471252, essv5582099
SamplesNA19712, NA18511, HG01079, NA20759, NA19359, NA12828, HG01350, NA19144, NA19210, HG01204, HG00253, HG00188, HG01171, HG00250, NA12004, HG00638, NA12761, HG01136, NA20589, HG00108, NA12716, NA19129, NA12892, HG00640, HG00325, NA20795, NA12275, NA19005, HG00236, NA20810, NA19327, NA11993, NA20804, NA20517
Known GenesMPP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672420
Frequency
Sample Size1151
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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