A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948189



Internal ID18595035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113481699..113484665hg38UCSC Ensembl
Innerchr10:115241458..115244424hg19UCSC Ensembl
Innerchr10:115231448..115234414hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg382967
hg192967
hg182967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1868320, nssv1868313, nssv1868321, nssv1868314, nssv1868312, nssv1868318, nssv1868315, nssv1868316, nssv1868317, nssv1868319
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)nsv948189
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