A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033842



Internal ID18776375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39481806..40228945hg38UCSC Ensembl
Innerchr9:41626824..42373963hg19UCSC Ensembl
Innerchr9:41616824..42363959hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38747140
hg19747140
hg18747136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690242
Samples
Known GenesANKRD20A2, ANKRD20A3, KGFLP2, LOC643648, MGC21881
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033842
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