A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6674262



Internal ID10089324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:34614990..34615408hg38UCSC Ensembl
Outerchr17:32942009..32942427hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2715865
Supporting Variants
SamplesSSM031
Known GenesTMEM132E
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)essv6674262
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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