A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594473



Internal ID16381882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64334499..64397714hg38UCSC Ensembl
Innerchr4:65200217..65263432hg19UCSC Ensembl
Innerchr4:64882812..64946027hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3863216
hg1963216
hg1863216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1001630
Samples
Known GenesTECRL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594473
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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