A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631932



Internal ID7018742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44243648..44245548hg38UCSC Ensembl
Innerchr13:44243669..44245528hg38UCSC Ensembl
Outerchr13:44243628..44245569hg38UCSC Ensembl
chr13:44817784..44819684hg19UCSC Ensembl
Innerchr13:44817805..44819664hg19UCSC Ensembl
Outerchr13:44817764..44819705hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14710280, essv14710295, essv14710292, essv14710298, essv14710279, essv14710304, essv14710310, essv14710289, essv14710311, essv14710275, essv14710305, essv14710293, essv14710297, essv14710302, essv14710290, essv14710282, essv14710291, essv14710306, essv14710286, essv14710281, essv14710287, essv14710313, essv14710273, essv14710307, essv14710285, essv14710309, essv14710278, essv14710283, essv14710301, essv14710299, essv14710314, essv14710288, essv14710308, essv14710274, essv14710294, essv14710277, essv14710276, essv14710296, essv14710303, essv14710312, essv14710300, essv14710284
SamplesHG03812, HG03593, NA12842, HG03965, NA20508, HG01066, NA20752, HG02691, HG02688, HG03009, HG02687, HG02301, HG04070, NA21103, NA20759, HG03986, HG00106, HG03691, HG03649, HG03787, HG02334, NA21119, HG03775, NA21124, HG00331, HG03625, HG03991, HG03940, NA20522, HG04134, HG03809, HG00265, NA21123, NA21126, NA12347, NA20888, NA20868, NA20852, NA21133, HG04153, HG03867, NA21104
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631932
Frequency
Sample Size2504
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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