A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522861



Internal ID15450154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135629508..135630793hg38UCSC Ensembl
Innerchr9:138521354..138522639hg19UCSC Ensembl
Innerchr9:137661175..137662460hg18UCSC Ensembl
Innerchr9:135747299..135748584hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381286
hg191286
hg181286
hg171286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698516
Samples
Known GenesGLT6D1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522861
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