A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156088



Internal ID22086593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:91854224..92170137hg38UCSC Ensembl
Outerchr1:91852334..92176097hg38UCSC Ensembl
Innerchr1:92319781..92635694hg19UCSC Ensembl
Outerchr1:92317891..92641654hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38323764
hg19323764
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017912
Samples
Known GenesBRDT, BTBD8, EPHX4, KIAA1107, TGFBR3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156088
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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