A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6961382



Internal ID9720641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:42714745..42714919hg38UCSC Ensembl
Outerchr21:44134855..44135029hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2723567, esv2723568
Supporting Variants
SamplesSSM026
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)essv6961382
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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