A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639538



Internal ID18591133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133997524..134264464hg38UCSC Ensembl
Innerchr4:134918679..135185619hg19UCSC Ensembl
Innerchr4:135138129..135405069hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38266941
hg19266941
hg18266941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024165
Supporting Variants
Samples
Known GenesPABPC4L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639538
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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