A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6887658



Internal ID10282550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:89483661..89483792hg38UCSC Ensembl
Outerchr9:92098576..92098707hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738738, esv2738737
Supporting Variants
SamplesSSM096
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)essv6887658
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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