A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036928



Internal ID19126147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135247933..135410880hg38UCSC Ensembl
Innerchr9:138139779..138302726hg19UCSC Ensembl
Innerchr9:137279600..137442547hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38162948
hg19162948
hg18162948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7726n100
Supporting Variantsnssv3696437
Samples
Known GenesC9orf62
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036928
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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