A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2736174



Internal ID9970506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46502909..46503271hg38UCSC Ensembl
Outerchr10:47036049..47036411hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6698532, essv6890989, essv6799883
SamplesSSM038, SSM097, SSM072
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2736174
Frequency
Sample Size96
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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