A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522988



Internal ID15450281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109764818..109767744hg38UCSC Ensembl
Innerchr1:110307440..110310366hg19UCSC Ensembl
Innerchr1:110108963..110111889hg18UCSC Ensembl
Innerchr1:110019482..110022408hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382927
hg192927
hg182927
hg172927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698658
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522988
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