A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984075



Internal ID18619265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57555984..57556681hg38UCSC Ensembl
Innerchr15:57848182..57848879hg19UCSC Ensembl
Innerchr15:55635474..55636171hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38698
hg19698
hg18698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2025153, nssv2025159, nssv2025156, nssv2025150, nssv2025158, nssv2025157, nssv2025154, nssv2025152, nssv2025155, nssv2025151
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)nsv984075
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