A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6963520



Internal ID9722566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:177467884..177468036hg38UCSC Ensembl
Outerchr5:176894885..176895037hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731194, esv2731196
Supporting Variants
SamplesSSM027
Known GenesDBN1
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)essv6963520
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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