A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595009



Internal ID16382418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106134539..106138778hg38UCSC Ensembl
Innerchr4:107055696..107059935hg19UCSC Ensembl
Innerchr4:107275145..107279384hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg384240
hg194240
hg184240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9193n54
Supporting Variantsnssv1003694
Samples
Known GenesTBCK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595009
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