A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6836581



Internal ID9889906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:152348822..152349129hg38UCSC Ensembl
Outerchr2:153205336..153205643hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2720967, esv2720968
Supporting Variants
SamplesSSM083
Known GenesFMNL2
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)essv6836581
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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