A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011885



Internal ID18754420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5091796..5119723hg38UCSC Ensembl
Innerchr4:5093523..5121450hg19UCSC Ensembl
Innerchr4:5144424..5172351hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3827928
hg1927928
hg1827928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738142
Samples
Known GenesSTK32B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011885
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