A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025903



Internal ID19115120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30112920..30213455hg38UCSC Ensembl
Innerchr9:30112918..30213453hg19UCSC Ensembl
Innerchr9:30102918..30203453hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38100536
hg19100536
hg18100536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688788
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025903
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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