A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593553



Internal ID16380962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7042597..7044033hg38UCSC Ensembl
Innerchr4:7044324..7045760hg19UCSC Ensembl
Innerchr4:7095225..7096661hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381437
hg191437
hg181437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8941n54
Supporting Variantsnssv990865
Samples
Known GenesCCDC96, LOC100129931, TADA2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593553
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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