A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6958447



Internal ID10066974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86758190..86758548hg38UCSC Ensembl
Outerchr9:89373105..89373463hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738697
Supporting Variants
SamplesSSM026
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)essv6958447
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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