A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1026060



Internal ID16320016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:14871739..14875759hg38UCSC Ensembl
Innerchr5:14871848..14875868hg19UCSC Ensembl
Innerchr5:14924848..14928868hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg384021
hg194021
hg184021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597258
Supporting Variants
Samples
Known GenesANKH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1026060
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