A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968678



Internal ID18603906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42913919..42988838hg38UCSC Ensembl
Innerchr9:66329727..66404638hg19UCSC Ensembl
Innerchr9:66069547..66144458hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3874920
hg1974912
hg1874912
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2546687, nssv2546683, nssv2546681, nssv2546684, nssv2546680, nssv2546679, nssv2546682, nssv2546685, nssv2546686, nssv2546678
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)nsv968678
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