A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976141



Internal ID18611348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91271127..91274282hg38UCSC Ensembl
Innerchr13:91923381..91926536hg19UCSC Ensembl
Innerchr13:90721382..90724537hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg383156
hg193156
hg183156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1970743, nssv1970745, nssv1970742, nssv1970746, nssv1970749, nssv1970748, nssv1970744, nssv1970740, nssv1970741, nssv1970747
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)nsv976141
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