A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522297



Internal ID15449590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130398878..130400192hg38UCSC Ensembl
Innerchr9:133274265..133275579hg19UCSC Ensembl
Innerchr9:132264086..132265400hg18UCSC Ensembl
Innerchr9:130303819..130305133hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381315
hg191315
hg181315
hg171315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695078
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522297
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