A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657768



Internal ID9923873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89707903..89708226hg38UCSC Ensembl
chr5:89003720..89004043hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5772685, essv5528292, essv5445623, essv6077337, essv5837599, essv6302620, essv6059300, essv5435774, essv5827542, essv6337638, essv5454022, essv6427362, essv5789475, essv5408270, essv6215437, essv6453552, essv6387845, essv6160530, essv6427809, essv5425190, essv6569514, essv5414860, essv6303571, essv5860489, essv6127015, essv5703475, essv6201859, essv6327979, essv5486900, essv6456785, essv5491416, essv5824278, essv6011203, essv5532522, essv5884836, essv5719787, essv5784632, essv6494489, essv5762779, essv5615622, essv5734745, essv6342214, essv6409547, essv5891433, essv6425426, essv6061483, essv5520998, essv5690332, essv5396840, essv6294508, essv5945298, essv6353281, essv5634910, essv5570797, essv6410399, essv6044212, essv6486329, essv6579970, essv5940633, essv5592906, essv6487812, essv6365002, essv5701052, essv6333070, essv6455220, essv6553089, essv6067757, essv6118891, essv5971884
SamplesNA19394, NA18502, HG01173, NA19700, NA19703, NA19397, NA18508, NA19399, HG01052, NA19332, HG01188, NA18917, NA19350, NA19359, NA18959, HG00115, NA19190, NA18870, NA20356, NA18510, NA12155, NA19396, NA19373, NA18519, NA19382, NA18489, NA19448, NA19138, NA18498, NA20336, NA19404, NA19720, NA19383, NA18868, NA19917, HG01072, NA19172, NA19901, NA19189, NA18520, NA19445, NA19985, NA18867, NA11993, HG01136, NA19707, NA12003, NA19347, NA18933, NA18516, NA19982, NA20344, NA18856, NA19099, NA19452, NA18523, NA19469, NA19390, NA19380, NA19428, NA18501, NA20348, NA19785, NA20334, NA19713, NA19093, NA19711, NA18505, NA18488
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657768
Frequency
Sample Size1151
Observed Gain0
Observed Loss69
Observed Complex0
Frequencyn/a


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