A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556382



Internal ID15997105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107778300..107826907hg38UCSC Ensembl
Innerchr11:107649026..107697633hg19UCSC Ensembl
Innerchr11:107154236..107202843hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3848608
hg1948608
hg1848608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2175n54
Supporting Variantsnssv1174953
SamplesHGDP01166
Known GenesSLC35F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556382
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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