A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6969736



Internal ID9728718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100610855..100611451hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734888, esv2734903
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)essv6969736
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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