A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2738899



Internal ID10322535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:107716347..107716702hg38UCSC Ensembl
Outerchr9:110478628..110478983hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6912158, essv6970302
SamplesSSM028, SSM015
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)esv2738899
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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