A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977276



Internal ID18612482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103599669..103606449hg38UCSC Ensembl
Innerchr13:104252019..104258799hg19UCSC Ensembl
Innerchr13:103050020..103056800hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg386781
hg196781
hg186781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1974698, nssv1974696, nssv1974689, nssv1974692, nssv1974690, nssv1974691, nssv1974693, nssv1974697, nssv1974695, nssv1974694
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977276
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