A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633501



Internal ID6673623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108239215..108256002hg38UCSC Ensembl
Innerchr13:108239365..108255852hg38UCSC Ensembl
Outerchr13:108239065..108256152hg38UCSC Ensembl
chr13:108891563..108908350hg19UCSC Ensembl
Innerchr13:108891713..108908200hg19UCSC Ensembl
Outerchr13:108891413..108908500hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3816788
hg1916788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14893585, essv14893586, essv14893588, essv14893587, essv14893592, essv14893590, essv14893593, essv14893591, essv14893589
SamplesHG04156, HG03706, HG02490, HG04106, HG02737, HG04162, NA20862, HG03823, HG04141
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633501
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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