A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974571



Internal ID18609782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48969389..48973471hg38UCSC Ensembl
Innerchr15:49261586..49265668hg19UCSC Ensembl
Innerchr15:47048878..47052960hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg384083
hg194083
hg184083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2023704, nssv2023702, nssv2023706, nssv2023703, nssv2023710, nssv2023701, nssv2023705, nssv2023709, nssv2023707, nssv2023708
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)nsv974571
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