A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2747357



Internal ID9981641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:46332526..46333425hg38UCSC Ensembl
Outerchr13:46906661..46907560hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6977505, essv6966045, essv6851449, essv6772218, essv6673392, essv6819883, essv6755691, essv6857446, essv6735296, essv6867350, essv6712077, essv6862571
SamplesSSM027, SSM065, SSM087, SSM088, SSM058, SSM029, SSM089, SSM031, SSM086, SSM006, SSM078, SSM049
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)esv2747357
Frequency
Sample Size96
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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