A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627831



Internal ID7014656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116809983..116813169hg38UCSC Ensembl
Innerchr11:116810003..116813150hg38UCSC Ensembl
Outerchr11:116809964..116813189hg38UCSC Ensembl
chr11:116680699..116683885hg19UCSC Ensembl
Innerchr11:116680719..116683866hg19UCSC Ensembl
Outerchr11:116680680..116683905hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383187
hg193187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14291956, essv14291947, essv14291935, essv14291949, essv14291972, essv14291952, essv14291934, essv14291961, essv14291967, essv14291966, essv14291942, essv14291938, essv14291937, essv14291939, essv14291971, essv14291954, essv14291945, essv14291950, essv14291962, essv14291944, essv14291946, essv14291958, essv14291940, essv14291955, essv14291941, essv14291970, essv14291953, essv14291964, essv14291943, essv14291968, essv14291936, essv14291973, essv14291960, essv14291959, essv14291957, essv14291965, essv14291948, essv14291951, essv14291969, essv14291963
SamplesHG01402, HG03228, HG04222, HG01052, HG03229, NA20771, NA07357, HG01070, HG03705, HG03722, HG03976, HG04182, HG03594, HG03986, HG02224, NA20896, NA20811, NA20755, HG01164, HG04062, HG04107, HG03742, NA20867, HG03631, HG03643, HG01593, HG03634, HG03752, HG02660, HG01253, HG03727, HG03108, NA21125, NA20888, HG02053, HG04098, NA20886, HG03922, NA12890, HG01618
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627831
Frequency
Sample Size2504
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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