A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977904



Internal ID18613109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11240738..11245382hg38UCSC Ensembl
Innerchr16:11334595..11339239hg19UCSC Ensembl
Innerchr16:11242096..11246740hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg384645
hg194645
hg184645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2043729, nssv2043735, nssv2043732, nssv2043734, nssv2043726, nssv2043728, nssv2043733, nssv2043730, nssv2043731, nssv2043727
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)nsv977904
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