A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169468



Internal ID21313951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:57877338..57881771hg38UCSC Ensembl
Outerchr11:57874411..57885339hg38UCSC Ensembl
Innerchr11:57644810..57649243hg19UCSC Ensembl
Outerchr11:57641883..57652811hg19UCSC Ensembl
Innerchr11:57401386..57405819hg18UCSC Ensembl
Outerchr11:57398459..57409387hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3810929
hg1910929
hg1810929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245952
SamplesMLY_9
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169468
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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