A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6800996



Internal ID9857324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:68035300..68035689hg38UCSC Ensembl
Outerchr17:66031416..66031805hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716136, esv2716138
Supporting Variants
SamplesSSM072
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)essv6800996
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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