A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155771



Internal ID22086276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87134049..87287255hg38UCSC Ensembl
Outerchr2:87117615..87287267hg38UCSC Ensembl
Innerchr2:87361172..87514378hg19UCSC Ensembl
Outerchr2:87344738..87514390hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38169653
hg19169653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011362
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155771
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