A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6969732



Internal ID10075408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98547918..98548552hg38UCSC Ensembl
Outerchr7:98177230..98177864hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734869
Supporting Variants
SamplesSSM028
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)essv6969732
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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