A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673844



Internal ID9593263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129680527..129680645hg38UCSC Ensembl
chr10:131478791..131478909hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5964007, essv6421264, essv6124224, essv5757191, essv6280480, essv5815523, essv5946969, essv6445041, essv6566310, essv6086656, essv6320042, essv5987075, essv5546818, essv5992003, essv5972711, essv6531649, essv6368977, essv6050454, essv6286931, essv5839126
SamplesHG01357, NA20796, HG00375, HG00111, HG01107, HG01183, HG01136, HG00254, HG00237, NA12144, HG01497, HG01073, HG00246, HG01334, HG00281, HG01366, HG01125, NA20528, HG01374, HG00137
Known GenesMGMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673844
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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