A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6961375



Internal ID10067320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:42078125..42078231hg38UCSC Ensembl
Outerchr21:43498234..43498340hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2723516, esv2723518
Supporting Variants
SamplesSSM026
Known GenesUMODL1
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)essv6961375
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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