A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6925070



Internal ID10031837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:82614024..82614538hg38UCSC Ensembl
Outerchr17:80571900..80572414hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716511, esv2716512
Supporting Variants
SamplesSSM018
Known Genes
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)essv6925070
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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