A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2175n54



Internal ID20135599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107773570..107826907hg38UCSC Ensembl
chr11:107644296..107697633hg19UCSC Ensembl
chr11:107149506..107202843hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3853338
hg1953338
hg1853338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556381, nsv556382
SamplesHGDP01166
Known GenesSLC35F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2175n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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