A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6924367



Internal ID10033746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:51198969..51199383hg38UCSC Ensembl
Outerchr12:51592752..51593166hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745880
Supporting Variants
SamplesSSM018
Known GenesPOU6F1
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)essv6924367
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