A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6677872



Internal ID10091562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:93501016..93501699hg38UCSC Ensembl
Outerchr12:93894792..93895475hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746217
Supporting Variants
SamplesSSM032
Known GenesMRPL42
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)essv6677872
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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