A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6691258



Internal ID9757690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134262761..134262972hg38UCSC Ensembl
Outerchr9:137154607..137154818hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739205, esv2739138, esv2739204
Supporting Variants
SamplesSSM036
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)essv6691258
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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