A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6931397



Internal ID9693926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134262429..134263166hg38UCSC Ensembl
Outerchr9:137154275..137155012hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739138, esv2739204
Supporting Variants
SamplesSSM020
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)essv6931397
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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