A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6728139



Internal ID10138807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133111901..133112099hg38UCSC Ensembl
Outerchr10:134925405..134925603hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743821, esv2743817
Supporting Variants
SamplesSSM046
Known GenesGPR123
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)essv6728139
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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