A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6937793



Internal ID10046521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:158757144..158758111hg38UCSC Ensembl
Outerchr1:158726934..158727901hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38968
hg19968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718629
Supporting Variants
SamplesSSM022
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)essv6937793
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