A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6906103



Internal ID10021045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:21981201..22005811hg38UCSC Ensembl
Outerchr1:22307694..22332304hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3824611
hg1924611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745130
Supporting Variants
SamplesSSM014
Known GenesCELA3A, CELA3B
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)essv6906103
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