A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893693



Internal ID19184513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:48039242..48099144hg38UCSC Ensembl
Outerchr3:48039242..48099144hg38UCSC Ensembl
Innerchr3:48080732..48140634hg19UCSC Ensembl
Outerchr3:48080732..48140634hg19UCSC Ensembl
Innerchr3:48055736..48115638hg18UCSC Ensembl
Outerchr3:48055736..48115638hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3859903
hg1959903
hg1859903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786987
Samples
Known GenesMAP4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893693
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