A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892416



Internal ID19183236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88321158..88372044hg38UCSC Ensembl
Outerchr13:88321158..88372044hg38UCSC Ensembl
Innerchr13:88973413..89024299hg19UCSC Ensembl
Outerchr13:88973413..89024299hg19UCSC Ensembl
Innerchr13:87771414..87822300hg18UCSC Ensembl
Outerchr13:87771414..87822300hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3850887
hg1950887
hg1850887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782033
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892416
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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