A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6789037



Internal ID9846364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:42283566..42283671hg38UCSC Ensembl
Outerchr21:43703676..43703781hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2723543, esv2723541, esv2723542
Supporting Variants
SamplesSSM069
Known GenesABCG1
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)essv6789037
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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