A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483071



Internal ID15582184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:123919556..124090911hg38UCSC Ensembl
Innerchr4:124840711..125012066hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38171356
hg19171356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2995990
Samples
Known GenesLINC01091
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483071
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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