A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2738998



Internal ID9973339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:121077739..121077849hg38UCSC Ensembl
Outerchr9:123840017..123840127hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6672464
SamplesSSM031
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)esv2738998
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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