A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982226



Internal ID18617421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60854928..60879309hg38UCSC Ensembl
Innerchr9:39825166..39849841hg19UCSC Ensembl
Innerchr9:39815166..39839841hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3824382
hg1924676
hg1824676
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2530873, nssv2530877, nssv2530881, nssv2530880, nssv2530878, nssv2530882, nssv2530879, nssv2530874, nssv2530875, nssv2530876
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)nsv982226
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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