A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982354



Internal ID18617549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137057355..137073859hg38UCSC Ensembl
Innerchr9:139951807..139968311hg19UCSC Ensembl
Innerchr9:139071628..139088132hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3816505
hg1916505
hg1816505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2570502, nssv2570496, nssv2570498, nssv2570493, nssv2570501, nssv2570495, nssv2570499, nssv2570500, nssv2570494, nssv2570497
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSAPCD2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982354
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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