A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526397



Internal ID15453690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102256798..102262486hg38UCSC Ensembl
Innerchr9:105019080..105024768hg19UCSC Ensembl
Innerchr9:104058901..104064589hg18UCSC Ensembl
Innerchr9:102098635..102104323hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385689
hg195689
hg185689
hg175689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702696
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526397
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