A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660529



Internal ID9926634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104151378..104151970hg38UCSC Ensembl
chr3:103870222..103870814hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5718280, essv5480058, essv6586133, essv5526460, essv6269359, essv6261203, essv6554482, essv5846963, essv6133604, essv6077857, essv5987092, essv6309785, essv5755998, essv6434806, essv6502385, essv6580923, essv6144975, essv6181350, essv5878718, essv6190120, essv6280537, essv6276839, essv6105480, essv5700872, essv6240188, essv6160198, essv5715961, essv5875340, essv5574811, essv5648768, essv6510880, essv6586473, essv5629442, essv5578891, essv5483365, essv5878168, essv6384416, essv5537485, essv6166923, essv5959217
SamplesNA18621, HG00524, NA18561, NA18599, NA18603, NA18596, NA18627, NA19076, NA18940, HG00501, HG00634, HG00156, HG00705, HG00419, NA18614, NA19077, NA18991, HG00475, HG00533, HG00500, NA18579, NA18566, HG00404, HG00479, NA18634, HG00476, NA18543, HG00565, NA19072, HG01375, HG00662, HG00707, NA18987, HG00698, NA18552, HG00472, NA19074, NA18622, NA18577, HG00593
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660529
Frequency
Sample Size1151
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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