A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2747399



Internal ID10328369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:49799281..49799934hg38UCSC Ensembl
Outerchr13:50373417..50374070hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6815592, essv6945115, essv6792005, essv6803614
SamplesSSM073, SSM023, SSM077, SSM070
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)esv2747399
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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