A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6833669



Internal ID9886911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:666380..667824hg38UCSC Ensembl
Outerchr6:666380..667824hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381445
hg191445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731368
Supporting Variants
SamplesSSM082
Known GenesEXOC2
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)essv6833669
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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