A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891941



Internal ID19186337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20618318..20627519hg38UCSC Ensembl
Outerchr11:20618318..20627519hg38UCSC Ensembl
Innerchr11:20639864..20649065hg19UCSC Ensembl
Outerchr11:20639864..20649065hg19UCSC Ensembl
Innerchr11:20596440..20605641hg18UCSC Ensembl
Outerchr11:20596440..20605641hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg389202
hg199202
hg189202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779071
Samples
Known GenesSLC6A5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891941
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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