A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623133



Internal ID7009990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46274728..46325913hg38UCSC Ensembl
chr10:47645964..47697149hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3851186
hg1951186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13785822, essv13785824, essv13785820, essv13785819, essv13785825, essv13785823, essv13785826, essv13785821, essv13785827
SamplesNA20339, HG03378, NA18861, HG03499, HG04238, HG01882, NA11840, HG00237, NA19248
Known GenesANTXRL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623133
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