A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6888933



Internal ID10013304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:153611072..153611764hg38UCSC Ensembl
Outerchr6:153932207..153932899hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732927
Supporting Variants
SamplesSSM012
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)essv6888933
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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