A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6865456



Internal ID10262392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:910437..910708hg38UCSC Ensembl
Outerchr6:910787..910980hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38272
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731402, esv2731403
Supporting Variants
SamplesSSM089
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)essv6865456
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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