A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6671360



Internal ID10086273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:168316298..168316427hg38UCSC Ensembl
Outerchr6:168716978..168717107hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733338, esv2733341, esv2733340
Supporting Variants
SamplesSSM031
Known GenesDACT2
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)essv6671360
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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