A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519890



Internal ID15447183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85970099..85982347hg38UCSC Ensembl
Innerchr9:88585014..88597262hg19UCSC Ensembl
Innerchr9:87774834..87787082hg18UCSC Ensembl
Innerchr9:85814568..85826816hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3812249
hg1912249
hg1812249
hg1712249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659321, nssv686125
Samples
Known GenesNAA35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519890
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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