A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019695



Internal ID19108913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30419932..30563356hg38UCSC Ensembl
Innerchr9:30419930..30563354hg19UCSC Ensembl
Innerchr9:30409930..30553354hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38143425
hg19143425
hg18143425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7504n100
Supporting Variantsnssv3688812, nssv3755916, nssv3688809, nssv3688818, nssv3688815, nssv3755915, nssv3755917, nssv3688817, nssv3755914, nssv3688810, nssv3688816, nssv3688813, nssv3688814, nssv3688811
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)nsv1019695
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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