A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6799026



Internal ID10204197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:168316675..168317882hg38UCSC Ensembl
Outerchr6:168717355..168718562hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381208
hg191208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733346, esv2733342, esv2733344
Supporting Variants
SamplesSSM072
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)essv6799026
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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