A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6697716



Internal ID10112176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:1768946..1769143hg38UCSC Ensembl
Outerchr5:1769061..1769258hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729531, esv2729530
Supporting Variants
SamplesSSM038
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)essv6697716
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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