A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039801



Internal ID18782332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104053295..104090136hg38UCSC Ensembl
Innerchr9:106815576..106852417hg19UCSC Ensembl
Innerchr9:105855397..105892238hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3836842
hg1936842
hg1836842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7695n100
Supporting Variantsnssv3697631
Samples
Known GenesMIR6130
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039801
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