A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981198



Internal ID18616397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153938332..153939615hg38UCSC Ensembl
Innerchr6:154259467..154260750hg19UCSC Ensembl
Innerchr6:154301160..154302443hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381284
hg191284
hg181284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2428213, nssv2428214, nssv2428215, nssv2428216, nssv2428208, nssv2428209, nssv2428217, nssv2428210, nssv2428211, nssv2428212
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)nsv981198
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