A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892308



Internal ID19183128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:22108511..22136338hg38UCSC Ensembl
Outerchr13:22108511..22136338hg38UCSC Ensembl
Innerchr13:22682650..22710477hg19UCSC Ensembl
Outerchr13:22682650..22710477hg19UCSC Ensembl
Innerchr13:21580650..21608477hg18UCSC Ensembl
Outerchr13:21580650..21608477hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3827828
hg1927828
hg1827828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779560
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892308
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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