A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6865327



Internal ID10262276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:77752517..77752844hg38UCSC Ensembl
Outerchr5:77048341..77048668hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2730329
Supporting Variants
SamplesSSM089
Known GenesTBCA
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)essv6865327
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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