A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892324



Internal ID19183144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31942334..31961859hg38UCSC Ensembl
Outerchr13:31942334..31961859hg38UCSC Ensembl
Innerchr13:32516471..32535996hg19UCSC Ensembl
Outerchr13:32516471..32535996hg19UCSC Ensembl
Innerchr13:31414471..31433996hg18UCSC Ensembl
Outerchr13:31414471..31433996hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3819526
hg1919526
hg1819526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783305
Samples
Known GenesEEF1DP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892324
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer