A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6957696



Internal ID10066298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:156941323..156941465hg38UCSC Ensembl
Outerchr7:156734017..156734159hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735653, esv2735654
Supporting Variants
SamplesSSM026
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)essv6957696
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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