A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781567



Internal ID18821694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20412913..20441076hg38UCSC Ensembl
Innerchr13:20987052..21015215hg19UCSC Ensembl
Innerchr13:19885052..19913215hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3828164
hg1928164
hg1828164
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892302
Supporting Variants
Samples
Known GenesCRYL1, MIR4499
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781567
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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