A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016109



Internal ID18758644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6712314..6924843hg38UCSC Ensembl
Innerchr9:6712314..6924843hg19UCSC Ensembl
Innerchr9:6702314..6914843hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38212530
hg19212530
hg18212530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758109
Samples
Known GenesKDM4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016109
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