A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154728



Internal ID22085233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:221222983..221233091hg38UCSC Ensembl
Outerchr1:221220533..221237547hg38UCSC Ensembl
Innerchr1:221396325..221406433hg19UCSC Ensembl
Outerchr1:221393875..221410889hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3817015
hg1917015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007962
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154728
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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