A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519021



Internal ID15446314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121350798..121356019hg38UCSC Ensembl
Innerchr6:121671944..121677165hg19UCSC Ensembl
Innerchr6:121713643..121718864hg18UCSC Ensembl
Innerchr6:121713643..121718864hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg385222
hg195222
hg185222
hg175222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696492
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519021
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