A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155887



Internal ID22086392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:179423254..179433233hg38UCSC Ensembl
Outerchr2:179422429..179436541hg38UCSC Ensembl
Innerchr2:180287981..180297960hg19UCSC Ensembl
Outerchr2:180287156..180301268hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg3814113
hg1914113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015373, nssv4015372
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155887
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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