A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051091



Internal ID19140310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102144997..102217289hg38UCSC Ensembl
Innerchr9:104907279..104979571hg19UCSC Ensembl
Innerchr9:103947100..104019392hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3872293
hg1972293
hg1872293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697580
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)nsv1051091
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