A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974070



Internal ID18262597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26568347..26580345hg38UCSC Ensembl
Innerchr13:27142484..27154482hg19UCSC Ensembl
Innerchr13:26040484..26052482hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3811999
hg1911999
hg1811999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1957028, nssv1957025, nssv1957027, nssv1957032, nssv1957026, nssv1957030, nssv1957033, nssv1957034, nssv1957029, nssv1957031
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesWASF3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974070
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