A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661962



Internal ID9581381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122917875..122918925hg38UCSC Ensembl
chr11:122788583..122789633hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381051
hg191051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5863626, essv5995678, essv6180483, essv6574921, essv6299003, essv6002476, essv5773591, essv5834978, essv5934596, essv6461939, essv5907307, essv5716769, essv6060977, essv5803813, essv5743278, essv6193765, essv6005612, essv5521366, essv5403166, essv6153398, essv6455496, essv5482645, essv6385646, essv6574621, essv6443921, essv5420016, essv6526606, essv5907897, essv5903778, essv6116483, essv6064282, essv5700844, essv6136100
SamplesNA19625, NA19436, NA19712, NA18874, NA19093, NA20346, NA19317, NA19334, NA19788, NA19331, NA19449, NA19144, NA19379, NA18488, NA18960, NA19444, NA18916, NA19247, NA19313, NA20348, NA18486, NA18504, NA19704, NA19707, NA18974, NA19462, NA19431, NA19747, NA18924, NA19916, NA19130, NA19204, NA19200
Known GenesC11orf63
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661962
Frequency
Sample Size1151
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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