A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009488



Internal ID16303444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151331542..151347925hg38UCSC Ensembl
Innerchr4:152252694..152269077hg19UCSC Ensembl
Innerchr4:152472144..152488527hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3816384
hg1916384
hg1816384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595708
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1009488
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