A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982321



Internal ID18617516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92539232..92540093hg38UCSC Ensembl
Innerchr9:95301514..95302375hg19UCSC Ensembl
Innerchr9:94341335..94342196hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38862
hg19862
hg18862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2557850, nssv2557848, nssv2557846, nssv2557852, nssv2557847, nssv2557855, nssv2557851, nssv2557854, nssv2557853, nssv2557849
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCENPP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982321
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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