A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2973610



Internal ID15805719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39830214..39863126hg38UCSC Ensembl
Innerchr9:41975232..42008144hg19UCSC Ensembl
Innerchr9:41965232..41998144hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3832913
hg1932913
hg1832913
Variant TypeCNV gain
Copy Number13
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515141
Supporting Variants
SamplesNA21583
Known GenesKGFLP2, LOC643648
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2973610
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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