A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2738861



Internal ID9973202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:103014751..103014950hg38UCSC Ensembl
Outerchr9:105777033..105777232hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6879194, essv6908430
SamplesSSM093, SSM014
Known GenesCYLC2
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)esv2738861
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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