A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6686653



Internal ID10103459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:126534948..126535074hg38UCSC Ensembl
Outerchr3:126253791..126253917hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2725870, esv2725871
Supporting Variants
SamplesSSM035
Known GenesCHST13
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)essv6686653
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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