A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6821385



Internal ID9876042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:243338880..243339236hg38UCSC Ensembl
Outerchr1:243502182..243502538hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2726485
Supporting Variants
SamplesSSM079
Known GenesSDCCAG8
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)essv6821385
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