A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6903592



Internal ID9668631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:143284796..143285242hg38UCSC Ensembl
Outerchr5:142664361..142664807hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2730856
Supporting Variants
SamplesSSM013
Known GenesNR3C1
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)essv6903592
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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