A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2774151



Internal ID15731790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122631254..122633774hg38UCSC Ensembl
Innerchr10:124390770..124393290hg19UCSC Ensembl
Innerchr10:124380760..124383280hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382521
hg192521
hg182521
Variant TypeCNV gain
Copy Number14
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514542
Supporting Variants
SamplesNA19108
Known GenesDMBT1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2774151
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