A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948151



Internal ID18594997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:96558998..96561530hg38UCSC Ensembl
Innerchr10:98318755..98321287hg19UCSC Ensembl
Innerchr10:98308745..98311277hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382533
hg192533
hg182533
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1862515, nssv1862517, nssv1862520, nssv1862518, nssv1862516, nssv1862511, nssv1862512, nssv1862519, nssv1862513, nssv1862514
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTM9SF3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948151
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