A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982198



Internal ID18270707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19105114..19108547hg38UCSC Ensembl
Innerchr9:19105112..19108545hg19UCSC Ensembl
Innerchr9:19095112..19098545hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg383434
hg193434
hg183434
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2523751, nssv2523752, nssv2523749, nssv2523748, nssv2523756, nssv2523755, nssv2523750, nssv2523757, nssv2523753, nssv2523754
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)nsv982198
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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