A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976104



Internal ID18611311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:36938327..36939327hg38UCSC Ensembl
Innerchr13:37512464..37513464hg19UCSC Ensembl
Innerchr13:36410464..36411464hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1960573, nssv1960575, nssv1960571, nssv1960572, nssv1960567, nssv1960574, nssv1960566, nssv1960568, nssv1960569, nssv1960570
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)nsv976104
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