A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9520n54



Internal ID22777415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1008649..1009454hg38UCSC Ensembl
chr5:1008764..1009569hg19UCSC Ensembl
chr5:1061764..1062569hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38806
hg19806
hg18806
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596796, nsv596795, nsv596794
Samples
Known GenesNKD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9520n54
Frequency
Sample Size17421
Observed Gain10
Observed Loss4
Observed Complex0
Frequencyn/a


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