A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892321



Internal ID19183141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24982879..25019327hg38UCSC Ensembl
Outerchr13:24982879..25019327hg38UCSC Ensembl
Innerchr13:25557017..25593465hg19UCSC Ensembl
Outerchr13:25557017..25593465hg19UCSC Ensembl
Innerchr13:24455017..24491465hg18UCSC Ensembl
Outerchr13:24455017..24491465hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3836449
hg1936449
hg1836449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787525
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892321
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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