A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968726



Internal ID18603954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90206184..90236424hg38UCSC Ensembl
Innerchr9:92968466..92998706hg19UCSC Ensembl
Innerchr9:92008286..92038526hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3830241
hg1930241
hg1830241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2556861, nssv2556864, nssv2556863, nssv2556867, nssv2556868, nssv2556860, nssv2556862, nssv2556865, nssv2556866, nssv2556859
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)nsv968726
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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