A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6885386



Internal ID9933467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:13200626..13202598hg38UCSC Ensembl
Outerchr16:13294483..13296455hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381973
hg191973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2713995
Supporting Variants
SamplesSSM095
Known GenesSHISA9
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)essv6885386
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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