A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2930986



Internal ID15738090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257332..380527hg38UCSC Ensembl
Innerchr6:257332..380527hg19UCSC Ensembl
Innerchr6:202332..325527hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38123196
hg19123196
hg18123196
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514340
Supporting Variants
SamplesNA19128
Known GenesDUSP22
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2930986
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