A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156216



Internal ID22086721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15162689..15163790hg38UCSC Ensembl
Outerchr1:15159958..15167414hg38UCSC Ensembl
Innerchr1:15489185..15490286hg19UCSC Ensembl
Outerchr1:15486454..15493910hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg387457
hg197457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4019126
Samples
Known GenesC1orf195, TMEM51
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156216
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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