A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6779632



Internal ID9653084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:76792501..76793076hg38UCSC Ensembl
Outerchr18:74504457..74505032hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717416, esv2717388
Supporting Variants
SamplesSSM008
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)essv6779632
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