A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595420



Internal ID16382829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130607042..130708805hg38UCSC Ensembl
Innerchr4:131528197..131629960hg19UCSC Ensembl
Innerchr4:131747647..131849410hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38101764
hg19101764
hg18101764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9265n54
Supporting Variantsnssv1006489
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595420
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