A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6835643



Internal ID10006139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:132564592..132564832hg38UCSC Ensembl
Outerchr12:133141178..133141418hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747019
Supporting Variants
SamplesSSM010
Known GenesFBRSL1
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)essv6835643
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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