A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6975100



Internal ID10082880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170253318..170253410hg38UCSC Ensembl
Outerchr6:170562406..170562498hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733600, esv2733599, esv2733563
Supporting Variants
SamplesSSM029
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)essv6975100
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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