A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6779059



Internal ID9837948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134457194..134457574hg38UCSC Ensembl
Outerchr9:137349040..137349420hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739210, esv2739138
Supporting Variants
SamplesSSM067
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)essv6779059
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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