A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155636



Internal ID22086141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:716956..1042136hg38UCSC Ensembl
Outerchr20:714250..1047464hg38UCSC Ensembl
Innerchr20:697600..1022779hg19UCSC Ensembl
Outerchr20:694894..1028107hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38333215
hg19333214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013738
Samples
Known GenesANGPT4, FAM110A, RSPO4, SLC52A3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155636
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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