A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6708699



Internal ID9775492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100610916..100611411hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg19496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734906, esv2734888, esv2734903
Supporting Variants
SamplesSSM041
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)essv6708699
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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