A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6673356



Internal ID10090139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:26982837..26983167hg38UCSC Ensembl
Outerchr13:27556974..27557304hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747178
Supporting Variants
SamplesSSM031
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)essv6673356
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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