A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657839



Internal ID9923944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94889757..94890314hg38UCSC Ensembl
chr14:95356094..95356651hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5783994, essv6120953, essv6026940, essv5764108, essv6451928, essv5729633, essv5849187, essv5960083, essv5911480, essv6414941, essv6139356, essv5528383, essv5487242, essv5564365, essv5737168, essv5516980, essv6248393, essv5927635, essv6244946, essv6463195, essv6458570, essv6542091, essv6299931, essv5475509, essv6226608, essv5496014, essv5547956, essv5460282, essv5615936, essv5763244, essv5613229, essv5627927, essv5402509, essv5863707, essv6195055, essv6461600, essv6079413, essv5782405, essv6102743, essv5695522, essv6486218, essv6228204, essv6253966, essv5549978, essv6439199, essv6145170, essv5512872, essv6249560, essv5618529, essv6001741, essv5692417, essv5716022, essv6019577, essv5875664, essv6450749, essv6369678, essv5986803, essv5590195, essv5609543, essv6470742, essv5472375, essv6311103, essv5757139, essv6453716, essv5916752, essv5444483, essv5437321, essv5505434, essv6352341, essv6388360, essv5414216, essv6172689, essv5869262, essv6366601, essv6494645, essv5422023, essv5777715, essv6490032, essv6298556, essv6426139, essv5555025, essv5446672, essv6521428, essv5471957
SamplesNA19701, HG01173, NA20766, HG00361, NA18561, NA18507, NA11933, HG00306, NA20813, NA19377, NA18606, HG00737, NA20808, NA20507, NA20771, HG01140, HG00271, HG00641, HG01350, NA19005, NA18597, HG00702, HG00448, NA18567, NA20795, NA12348, HG00346, NA19457, NA19313, NA19088, HG00369, NA20513, NA19904, HG01134, NA12275, HG00148, NA12156, NA20812, NA19719, NA18986, NA12889, NA20811, HG01048, NA19451, NA20818, HG00149, HG00443, HG00266, NA20810, NA20760, NA20314, HG00275, NA20770, NA12234, HG00284, NA18573, HG00373, NA11894, HG01383, HG00157, NA18963, NA20828, HG00265, NA19834, NA19108, NA18559, HG00353, HG00098, NA20281, NA18610, NA12347, NA19398, NA12830, NA19102, NA20807, HG00280, HG00377, NA07000, NA19429, NA18622, NA18487, HG00553, NA18562, NA11832
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657839
Frequency
Sample Size1151
Observed Gain0
Observed Loss84
Observed Complex0
Frequencyn/a


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