A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051081



Internal ID18793612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128476086..128590082hg38UCSC Ensembl
Innerchr9:131238365..131352361hg19UCSC Ensembl
Innerchr9:130278186..130392182hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38113997
hg19113997
hg18113997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759826
Samples
Known GenesGLE1, ODF2, SPTAN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051081
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