A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892302



Internal ID18836436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20412913..20441076hg38UCSC Ensembl
Outerchr13:20412913..20441076hg38UCSC Ensembl
Innerchr13:20987052..21015215hg19UCSC Ensembl
Outerchr13:20987052..21015215hg19UCSC Ensembl
Innerchr13:19885052..19913215hg18UCSC Ensembl
Outerchr13:19885052..19913215hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3828164
hg1928164
hg1828164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781567
Samples
Known GenesCRYL1, MIR4499
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892302
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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