A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972410



Internal ID18607626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87422912..87425441hg38UCSC Ensembl
Innerchr9:90037827..90040356hg19UCSC Ensembl
Innerchr9:89227647..89230176hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382530
hg192530
hg182530
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2555866, nssv2555860, nssv2555864, nssv2555862, nssv2555867, nssv2555868, nssv2555863, nssv2555861, nssv2555859, nssv2555865
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)nsv972410
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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