A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625262



Internal ID7012097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6168439..6171798hg38UCSC Ensembl
Innerchr11:6168443..6171794hg38UCSC Ensembl
Outerchr11:6168435..6171802hg38UCSC Ensembl
chr11:6189669..6193028hg19UCSC Ensembl
Innerchr11:6189673..6193024hg19UCSC Ensembl
Outerchr11:6189665..6193032hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383360
hg193360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14009035, essv14009016, essv14009025, essv14009023, essv14009020, essv14009039, essv14009017, essv14009026, essv14009010, essv14009019, essv14009022, essv14009031, essv14009033, essv14009042, essv14009028, essv14009034, essv14009013, essv14009030, essv14009043, essv14009027, essv14009012, essv14009037, essv14009041, essv14009015, essv14009024, essv14009029, essv14009038, essv14009011, essv14009014, essv14009021, essv14009036, essv14009032, essv14009040, essv14009018
SamplesHG02574, HG03484, NA19204, HG01885, HG03175, NA18881, HG02891, NA18504, NA19314, HG03478, HG03095, NA18489, HG03370, HG02642, HG02471, NA19159, NA19239, NA18864, HG03394, HG02477, HG01989, HG03081, HG03388, HG03078, HG03446, HG03567, HG02807, NA19147, NA20276, NA19144, NA18865, HG03433, HG02095, NA19129
Known GenesOR52B2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625262
Frequency
Sample Size2504
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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