A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6941026



Internal ID10048910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:844137..844499hg38UCSC Ensembl
Outerchr17:747377..747739hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2715372, esv2715373
Supporting Variants
SamplesSSM022
Known GenesNXN
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)essv6941026
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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