A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973255



Internal ID18608470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65169757..65189964hg38UCSC Ensembl
Innerchr9:42812305..42832350hg19UCSC Ensembl
Innerchr9:42802301..42822346hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3820208
hg1920046
hg1820046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2732373, nssv2732375, nssv2732368, nssv2732372, nssv2732369, nssv2732370, nssv2732377, nssv2732371, nssv2732374, nssv2732376
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973255
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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