A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520585



Internal ID15447878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153228538..153307183hg38UCSC Ensembl
Innerchr6:153549673..153628318hg19UCSC Ensembl
Innerchr6:153591366..153670011hg18UCSC Ensembl
Innerchr6:153641787..153720432hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3878646
hg1978646
hg1878646
hg1778646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697504
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520585
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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