A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2729465



Internal ID9963780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:1275680..1277009hg38UCSC Ensembl
Outerchr5:1275795..1277124hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381330
hg191330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6829897, essv6748502, essv6893229, essv6670653, essv6822182, essv6693868, essv6969062, essv6956510, essv6963224, essv6974236, essv6676254, essv6963225, essv6817825, essv6918460
SamplesSSM027, SSM079, SSM028, SSM029, SSM026, SSM017, SSM032, SSM031, SSM081, SSM078, SSM037, SSM098, SSM056
Known GenesTERT
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)esv2729465
Frequency
Sample Size96
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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