A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6868601



Internal ID10265221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:8757880..9323868hg38UCSC Ensembl
Outerchr21:9646713..10162701hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38565989
hg19515989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2723012
Supporting Variants
SamplesSSM089
Known GenesMIR3648, MIR3687, TEKT4P2
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)essv6868601
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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