A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6932495



Internal ID9691786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75395862..75396756hg38UCSC Ensembl
Outerchr16:75429760..75430654hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38895
hg19895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2714708
Supporting Variants
SamplesSSM020
Known GenesCFDP1
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)essv6932495
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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