A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525255



Internal ID15452548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31266604..31273255hg38UCSC Ensembl
Innerchr6:31234381..31241032hg19UCSC Ensembl
Innerchr6:31342360..31349011hg18UCSC Ensembl
Innerchr6:31342360..31349011hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg386652
hg196652
hg186652
hg176652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701352
Samples
Known GenesHLA-C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525255
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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