A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6720897



Internal ID10130720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:110385343..110386182hg38UCSC Ensembl
Outerchr13:111037690..111038529hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2748010
Supporting Variants
SamplesSSM044
Known GenesCOL4A2
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)essv6720897
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