A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972790



Internal ID18608006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97012395..97026333hg38UCSC Ensembl
Innerchr9:99774677..99788615hg19UCSC Ensembl
Innerchr9:98814498..98828436hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3813939
hg1913939
hg1813939
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2561025, nssv2561023, nssv2561026, nssv2561019, nssv2561027, nssv2561024, nssv2561018, nssv2561020, nssv2561022, nssv2561021
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHIATL2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972790
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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