A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626178



Internal ID7013012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45822613..45823853hg38UCSC Ensembl
Innerchr11:45822613..45823853hg38UCSC Ensembl
Outerchr11:45822337..45824384hg38UCSC Ensembl
chr11:45844164..45845404hg19UCSC Ensembl
Innerchr11:45844164..45845404hg19UCSC Ensembl
Outerchr11:45843888..45845935hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381241
hg191241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14118552, essv14118563, essv14118539, essv14118562, essv14118564, essv14118537, essv14118558, essv14118567, essv14118555, essv14118543, essv14118551, essv14118569, essv14118561, essv14118541, essv14118559, essv14118554, essv14118550, essv14118548, essv14118546, essv14118557, essv14118545, essv14118565, essv14118538, essv14118553, essv14118570, essv14118549, essv14118547, essv14118566, essv14118556, essv14118540, essv14118560, essv14118568, essv14118542, essv14118544
SamplesHG02658, NA19664, NA11933, NA20532, NA20321, HG00115, HG01682, HG01167, HG00238, HG01083, HG03917, HG01110, HG00277, HG01757, HG00232, NA20515, NA10847, HG01684, HG00551, HG01777, HG01094, HG02657, HG00099, NA20872, NA19019, HG00638, NA20804, NA20527, NA20778, HG02238, NA20510, HG00252, NA20503, NA20502
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626178
Frequency
Sample Size2504
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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