A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016146



Internal ID22077777
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155909
Supporting Variants
Samples
Known GenesNBEAL1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016146
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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