A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038962



Internal ID19128181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:118320206..118365224hg38UCSC Ensembl
Innerchr9:121082484..121127502hg19UCSC Ensembl
Innerchr9:120122305..120167323hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3845019
hg1945019
hg1845019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695207
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)nsv1038962
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