A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6861763



Internal ID10258601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:13571335..13575803hg38UCSC Ensembl
Outerchr9:13571334..13575802hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg384469
hg194469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738215
Supporting Variants
SamplesSSM088
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)essv6861763
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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