A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6920931



Internal ID9684428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:31332585..31332921hg38UCSC Ensembl
Outerchr17:29659603..29659939hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2715817
Supporting Variants
SamplesSSM017
Known GenesNF1
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)essv6920931
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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