A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948146



Internal ID18248306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95590762..95597378hg38UCSC Ensembl
Innerchr10:97350519..97357135hg19UCSC Ensembl
Innerchr10:97340509..97347125hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg386617
hg196617
hg186617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1862627, nssv1862629, nssv1862636, nssv1862633, nssv1862635, nssv1862631, nssv1862628, nssv1862630, nssv1862632, nssv1862634
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)nsv948146
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