A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126539



Internal ID15633039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6620059..6750556hg38UCSC Ensembl
Innerchr9:6620059..6750556hg19UCSC Ensembl
Innerchr9:6610059..6740556hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38130498
hg19130498
hg18130498
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613209
Supporting Variants
Samples
Known GenesGLDC, KDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126539
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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