A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2746902



Internal ID9981186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:131845016..131845176hg38UCSC Ensembl
Outerchr12:132329561..132329721hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6977399
SamplesSSM029
Known GenesMMP17
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)esv2746902
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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