A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6922982



Internal ID10032204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:23101146..23103765hg38UCSC Ensembl
Outerchr6:23101374..23103993hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382620
hg192620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731700
Supporting Variants
SamplesSSM018
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)essv6922982
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