A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6913362



Internal ID9638234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:11826062..11826819hg38UCSC Ensembl
Outerchr18:11826061..11826818hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716803
Supporting Variants
SamplesSSM002
Known GenesGNAL
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)essv6913362
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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