A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2207n54



Internal ID22770102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134469738..134876236hg38UCSC Ensembl
chr11:134339632..134746130hg19UCSC Ensembl
chr11:133844842..134251340hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38406499
hg19406499
hg18406499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556656, nsv556622, nsv556615, nsv556623, nsv556647, nsv556628, nsv556618, nsv556619, nsv556645, nsv556634, nsv556631, nsv556630, nsv556635, nsv556639, nsv556648, nsv556621, nsv556626, nsv556636, nsv556650, nsv556616, nsv556637, nsv556643, nsv556613, nsv556651, nsv556633, nsv556640, nsv556632, nsv556629, nsv556654, nsv556614, nsv556649, nsv556627, nsv556646
Samples1780862484_A, 1782681210_A, 1780854445_A, 1780862540_A, NINDS_135, NINDS_147, 1780854467_A, 1780862388_A, 1798860280_A, HGDP00671
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2207n54
Frequency
Sample Size17421
Observed Gain53
Observed Loss0
Observed Complex0
Frequencyn/a


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