A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026149



Internal ID19115366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23127563..23157037hg38UCSC Ensembl
Innerchr9:23127562..23157036hg19UCSC Ensembl
Innerchr9:23117562..23147036hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3829475
hg1929475
hg1829475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690733
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)nsv1026149
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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