A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6698483



Internal ID9766330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:132821654..132822387hg38UCSC Ensembl
Outerchr9:135697041..135697774hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739138, esv2739143
Supporting Variants
SamplesSSM038
Known GenesAK8
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)essv6698483
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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