A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892301



Internal ID19183121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20401130..20514578hg38UCSC Ensembl
Outerchr13:20401130..20514578hg38UCSC Ensembl
Innerchr13:20975269..21088717hg19UCSC Ensembl
Outerchr13:20975269..21088717hg19UCSC Ensembl
Innerchr13:19873269..19986717hg18UCSC Ensembl
Outerchr13:19873269..19986717hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38113449
hg19113449
hg18113449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781514, essv25787321
Samples
Known GenesCRYL1, MIR4499
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892301
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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