A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6915788



Internal ID9680099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134254505..134254929hg38UCSC Ensembl
Outerchr9:137146351..137146775hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739138, esv2739203
Supporting Variants
SamplesSSM016
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)essv6915788
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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