A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595583



Internal ID16036306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139307207..139317207hg38UCSC Ensembl
Innerchr4:140228361..140238361hg19UCSC Ensembl
Innerchr4:140447811..140457811hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3810001
hg1910001
hg1810001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9292n54
Supporting Variantsnssv1008210, nssv1008211
Samples
Known GenesNAA15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595583
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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