A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972763



Internal ID18607979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81917099..81918195hg38UCSC Ensembl
Innerchr9:84532014..84533110hg19UCSC Ensembl
Innerchr9:83721834..83722930hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381097
hg191097
hg181097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2553794, nssv2553789, nssv2553788, nssv2553787, nssv2553786, nssv2553792, nssv2553793, nssv2553791, nssv2553785, nssv2553790
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSPATA31D5P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972763
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