A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526773



Internal ID15454066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12200957..12469893hg38UCSC Ensembl
Innerchr9:12200957..12469893hg19UCSC Ensembl
Innerchr9:12190957..12459893hg18UCSC Ensembl
Innerchr9:12190957..12459893hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38268937
hg19268937
hg18268937
hg17268937
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703125
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526773
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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