A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694346



Internal ID15430998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6620059..6750556hg38UCSC Ensembl
Innerchr9:6620059..6750556hg19UCSC Ensembl
Innerchr9:6610059..6740556hg18UCSC Ensembl
Innerchr9:6610059..6740556hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38130498
hg19130498
hg18130498
hg17130498
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519777
Supporting Variants
Samples
Known GenesGLDC, KDM4C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694346
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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