A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6844893



Internal ID10243886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32474497..32482789hg38UCSC Ensembl
Outerchr6:32442274..32450566hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg388293
hg198293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731844, esv2731839, esv2731841, esv2731842, esv2731843, esv2731835, esv2731837, esv2731845, esv2731836, esv2731834, esv2731838
Supporting Variants
SamplesSSM085
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)essv6844893
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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