A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155654



Internal ID22086159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47151467..47160290hg38UCSC Ensembl
Outerchr20:47148347..47161314hg38UCSC Ensembl
Innerchr20:45780106..45788929hg19UCSC Ensembl
Outerchr20:45776986..45789953hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3812968
hg1912968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv180n97
Supporting Variantsnssv4013896, nssv4013895, nssv4013891, nssv4013897, nssv4013894, nssv4013889, nssv4013893, nssv4013886, nssv4013888, nssv4013887, nssv4013898, nssv4013890, nssv4013892, nssv4013899
Samples
Known GenesEYA2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155654
Frequency
Sample Size131
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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