A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2723567



Internal ID9957867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:42714408..42715225hg38UCSC Ensembl
Outerchr21:44134518..44135335hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38818
hg19818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6933209, essv6703768, essv6707208, essv6839874, essv6824883, essv6666823, essv6810292, essv6871660, essv6937578, essv6801545, essv6729532, essv6950448, essv6859088, essv6750550, essv6885926, essv6946394, essv6877619, essv6668852, essv6821100, essv6686097, essv6961382, essv6925608, essv6972207, essv6804350, essv6692673, essv6967810, essv6761815, essv6949562, essv6675108, essv6863857, essv6679068, essv6689198, essv6901546, essv6725750, essv6797351
SamplesSSM027, SSM092, SSM036, SSM061, SSM040, SSM078, SSM088, SSM090, SSM031, SSM035, SSM072, SSM020, SSM071, SSM032, SSM039, SSM024, SSM045, SSM083, SSM100, SSM056, SSM028, SSM029, SSM003, SSM095, SSM030, SSM073, SSM021, SSM034, SSM087, SSM046, SSM023, SSM079, SSM075, SSM026, SSM018
Known GenesPDE9A
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)esv2723567
Frequency
Sample Size96
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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