A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945905



Internal ID18246069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:42498972..42527184hg38UCSC Ensembl
Innerchr1:42964643..42992855hg19UCSC Ensembl
Innerchr1:42737230..42765442hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3828213
hg1928213
hg1828213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1762312, nssv1762317, nssv1762313, nssv1762310, nssv1762319, nssv1762316, nssv1762318, nssv1762315, nssv1762314, nssv1762311
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)nsv945905
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