A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6945777



Internal ID9703507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:74732879..74733433hg38UCSC Ensembl
Outerchr17:72729018..72729572hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716232
Supporting Variants
SamplesSSM023
Known GenesRAB37
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)essv6945777
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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