A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892446



Internal ID19183266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109249649..109265014hg38UCSC Ensembl
Outerchr13:109249649..109265507hg38UCSC Ensembl
Innerchr13:109901997..109917362hg19UCSC Ensembl
Outerchr13:109901997..109917855hg19UCSC Ensembl
Innerchr13:108699998..108715363hg18UCSC Ensembl
Outerchr13:108699998..108715856hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3815859
hg1915859
hg1815859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801651, essv25781702, essv25801487
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892446
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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