A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050874



Internal ID18793405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116372164..116526045hg38UCSC Ensembl
Innerchr9:119134443..119288324hg19UCSC Ensembl
Innerchr9:118174264..118328145hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38153882
hg19153882
hg18153882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7707n100
Supporting Variantsnssv3695165
Samples
Known GenesASTN2, LOC100128505, PAPPA, PAPPA-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050874
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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