A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2742614



Internal ID9976898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:132304430..132305594hg38UCSC Ensembl
Outerchr12:132881016..132882180hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg381165
hg191165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv216e201
Supporting Variantsessv6894752
SamplesSSM098
Known GenesGALNT9
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)esv2742614
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer