A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977678



Internal ID18612884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25085433..25090321hg38UCSC Ensembl
Innerchr15:25330580..25335468hg19UCSC Ensembl
Innerchr15:22881673..22886561hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg384889
hg194889
hg184889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2012033, nssv2012032, nssv2012034, nssv2012037, nssv2012036, nssv2012041, nssv2012039, nssv2012040, nssv2012038, nssv2012035
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSNORD116-17, SNORD116-18, SNORD116-19, SNORD116-20, SNORD116-21, SNORD116-22
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977678
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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