A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892449



Internal ID19183269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113971527..114015726hg38UCSC Ensembl
Outerchr13:113971527..114015726hg38UCSC Ensembl
Innerchr13:114740938..114781202hg19UCSC Ensembl
Outerchr13:114740938..114781202hg19UCSC Ensembl
Innerchr13:113759040..113799304hg18UCSC Ensembl
Outerchr13:113759040..113799304hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3844200
hg1940265
hg1840265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800080
Samples
Known GenesRASA3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892449
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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