A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972755



Internal ID18261285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68368568..68410476hg38UCSC Ensembl
Innerchr9:70983484..71025392hg19UCSC Ensembl
Innerchr9:70173304..70215212hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3841909
hg1941909
hg1841909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2552098, nssv2552103, nssv2552102, nssv2552099, nssv2552101, nssv2552106, nssv2552105, nssv2552104, nssv2552097, nssv2552100
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesPGM5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972755
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