A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6712667



Internal ID9778488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137774227..137774496hg38UCSC Ensembl
Outerchr9:140668679..140668948hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739466
Supporting Variants
SamplesSSM042
Known GenesEHMT1
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)essv6712667
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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