A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674082



Internal ID9940187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:220727..220878hg38UCSC Ensembl
chr11:220727..220878hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5796181, essv6103061, essv6267219, essv6318581, essv5703288, essv6357923, essv5767064, essv5800717, essv5692407, essv5942693, essv5966560, essv6027897, essv6402326, essv6062096, essv5579184, essv5804295, essv6231883, essv5457519, essv5659795, essv6364202, essv5658500, essv6228724, essv5726773, essv5752586, essv5406107, essv6306501, essv5417781, essv5662032, essv5407035, essv5552290, essv6086602, essv5505847, essv6503376, essv6455581, essv5761910, essv5525144, essv5990657, essv5586146, essv5952641, essv5986910, essv6316887, essv6525129, essv5842913, essv5776412, essv5907780
SamplesNA18599, HG00315, HG00699, NA18530, HG00271, HG01366, HG01488, NA18558, HG01083, HG01365, HG00334, HG00139, HG00277, HG00335, HG00422, NA18557, HG00260, HG01353, HG00313, NA18544, HG00268, HG00328, HG00701, HG00436, HG00320, HG00584, HG01390, HG00273, HG00651, HG00690, HG00331, HG00525, HG00246, HG00285, HG00580, HG00278, HG00237, HG00339, HG00614, HG00656, HG00274, HG01082, NA18623, NA18577, NA18620
Known GenesSIRT3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674082
Frequency
Sample Size1151
Observed Gain0
Observed Loss45
Observed Complex0
Frequencyn/a


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