A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689093



Internal ID18640688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6701133..6770362hg38UCSC Ensembl
Innerchr9:6701133..6770362hg19UCSC Ensembl
Innerchr9:6691133..6760362hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3869230
hg1969230
hg1869230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021016
Supporting Variants
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)nssv3689093
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