A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6935626



Internal ID9697710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:103014485..103015020hg38UCSC Ensembl
Outerchr9:105776767..105777302hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738858, esv2738857
Supporting Variants
SamplesSSM021
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)essv6935626
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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