A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6787849



Internal ID10191980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:131582114..131583038hg38UCSC Ensembl
Outerchr12:132066659..132067583hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38925
hg19925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746877, esv2746835
Supporting Variants
SamplesSSM069
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)essv6787849
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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