A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593773



Internal ID16381182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16225971..16226670hg38UCSC Ensembl
Innerchr4:16227594..16228293hg19UCSC Ensembl
Innerchr4:15836692..15837391hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38700
hg19700
hg18700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8979n54
Supporting Variantsnssv993100
Samples
Known GenesTAPT1, TAPT1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593773
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