A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155909



Internal ID22086414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:203035077..203037323hg38UCSC Ensembl
Outerchr2:203032174..203039417hg38UCSC Ensembl
Innerchr2:203899800..203902046hg19UCSC Ensembl
Outerchr2:203896897..203904140hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg387244
hg197244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016143, nssv4016142, nssv4016141, nssv4016147, nssv4016144, nssv4016146
Samples
Known GenesNBEAL1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155909
Frequency
Sample Size131
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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