A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984086



Internal ID18619276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65769989..65771870hg38UCSC Ensembl
Innerchr15:66062327..66064208hg19UCSC Ensembl
Innerchr15:63849381..63851262hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381882
hg191882
hg181882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2026902, nssv2026910, nssv2026904, nssv2026903, nssv2026907, nssv2026906, nssv2026909, nssv2026905, nssv2026908, nssv2026911
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDENND4A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984086
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