A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038530



Internal ID19127749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131160048..131202087hg38UCSC Ensembl
Innerchr9:134035435..134077474hg19UCSC Ensembl
Innerchr9:133025256..133067295hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3842040
hg1942040
hg1842040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695286
Samples
Known GenesNUP214
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038530
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