A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156787



Internal ID22087188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:155219369..155231273hg38UCSC Ensembl
Outerchr1:155210675..155241876hg38UCSC Ensembl
Innerchr1:155189160..155201064hg19UCSC Ensembl
Outerchr1:155180466..155211667hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3831202
hg1931202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022956
Samples
Known GenesGBA, GBAP1, MTX1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156787
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer