A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6739086



Internal ID9803927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:48554660..48557729hg38UCSC Ensembl
Outerchr2:48781799..48784868hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg383070
hg193070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2720033
Supporting Variants
SamplesSSM052
Known GenesSTON1, STON1-GTF2A1L
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)essv6739086
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