A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6879194



Internal ID9928072
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 StatusS
Merged Variantsesv2738858, esv2738857, esv2738861
Supporting Variants
SamplesSSM093
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)essv6879194
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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