A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051953



Internal ID18794484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116669310..116736770hg38UCSC Ensembl
Innerchr9:119431589..119499049hg19UCSC Ensembl
Innerchr9:118471410..118538870hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3867461
hg1967461
hg1867461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7708n100
Supporting Variantsnssv3695170
Samples
Known GenesASTN2, TRIM32
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051953
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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