A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945860



Internal ID18592710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:29680322..29682470hg38UCSC Ensembl
Innerchr1:30153169..30155317hg19UCSC Ensembl
Innerchr1:29925756..29927904hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382149
hg192149
hg182149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1756898, nssv1756902, nssv1756897, nssv1756901, nssv1756903, nssv1756906, nssv1756899, nssv1756904, nssv1756900, nssv1756905
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)nsv945860
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